An object of this invention is to provide a streptavidin mutant reduced in affinity to the naturally-occurring biotin, and to provide a modified biotin which shows a high affinity to such streptavidin mutant reduced in affinity to the naturally-occurring biotin. This invention can provide a compound composed of a dimer of modified biotin, a streptavidin mutant, angsd usage of them.
|
2. A streptavidin mutant comprising an amino acid sequence represented by SEQ ID NO: 4.
1. A streptavidin mutant comprising an amino acid sequence in which Asn at amino acid residue 37 in the amino acid sequence represented by SEQ ID NO: 3 is substituted with other amino acid residue.
9. A therapeutic, or in vivo or in vitro diagnostic kit, comprising (a) a streptavidin mutant-molecular probe conjugate obtained by combining a streptavidin mutant comprising an amino acid sequence in which Asn at amino acid residue 37 in the amino acid sequence represented by SEQ ID NO: 3 is substituted with other amino acid residue, with a molecular probe; and (b) an in vivo or in vitro diagnostic substance, or a therapeutic substance, labeled with a compound represented by formula (1) below:
##STR00055##
wherein, each of X1a, X1b, X2a and x2b independently represents o or NH, each of Y1 and Y2 independently represents C or S, each of Z1 and Z2 independently represents o, S or NH, each of V1 and V2 independently represents S or S+—O−, each of n1 and n2 independently represents 0 or 1, each of m1 and m2 independently represents and integer from 1 to 10, and L represents a linking group.
4. A streptavidin mutant-molecular probe conjugate, obtained by combining the streptavidin mutant described in
5. The streptavidin mutant-molecular probe conjugate of
6. The streptavidin mutant-molecular probe conjugate of
7. The streptavidin mutant-molecular probe conjugate of
8. A therapeutic agent, or in vivo or in vitro diagnostic agent, comprising the streptavidin mutant-molecular probe conjugate described in
|
The present application is a Divisional of U.S. application Ser. No. 15/119,441, filed Aug. 17, 2016, which is a National stage of International Patent Application No. PCT/JP2015/054431, filed Feb. 18, 2015, which claims priority to Japanese Application No. 2014-212861, filed Oct. 17, 2014 and Japanese Application No. 2014-028525, filed Feb. 18, 2014, the contents of which are expressly incorporated by reference herein in their entireties.
This invention relates to compound composed of a dimer of modified biotin, a streptavidin mutant, and usage of them.
Avidin and biotin, or, streptavidin and biotin show a very strong affinity (Kd=10−15 to 10−14 M), which is one of the strongest interactions between two biomolecules. Today, the avidin/streptavidin-biotin interaction has been widely used in the fields of biochemistry, molecular biology, and medicine (Green, (1975), Adv. Protein Chem., 29: 85-133; Green, (1990), Methods Enzymol., 184: 51-67). Avidin is a basic glycoprotein derived from albumen, and has an isoelectric point above 10. Meanwhile, streptavidin is derived from Streptomyces (Streptomyces avidinii), has the isoelectric point at around the neutral point, and has no sugar chain. Both proteins can form a tetramer, and can bind one biotin molecule per one subunit. The molecular weight it at around 60 kDa.
In recent years, there has been proposed the pretargeting method, as a method of drug delivery making use of the high binding ability of avidin/streptavidin with biotin, combined with an antigen molecule (Hnatowich, (1987), J. Nucl. Med., 28, 1294-1302). Chicken avidin and bacterial streptavidin are, however, highly immunogenic to human body, and produces an anti-avidin/streptavidin antibody in the early stage after being administered to human. This has been an inhibiting factor against implementation of the pretargeting method (Paganelli, (1991), Cancer Res., 51, 5960-5966). As a solution to this problem, a low-immunogenic streptavidin has been reported (International Patent WO2010/095455).
Also the pretargeting method using bisbiotin (compound obtained by combining two biotin molecules with a linker) and a streptavidin mutant (Park et al., Clin. Cancer Res.; 17(23); 7373-82, 2011) has been reported. This method has successfully solved a problem of endogenous biotin, by using a streptavidin mutant having an amino acid mutation denoted as S45A or Y43A. More specifically, while the streptavidin mutant with S45A or Y43A can bind biotin only weakly as compared with the wild-type streptavidin, the streptavidin mutant becomes to bind more strongly with bisbiotin after being converted into a bis-form compound.
The low-immunogenic streptavidin described above, although reduced in the immunogenicity to human, still has affinity to endogenous biotin inhuman body, so that it would elevate the background level in diagnostic applications, or it would fail in achieving a disease-specific drug effect in therapeutic applications. It is therefore an object of this invention to provide a streptavidin mutant reduced in affinity to the natural-occurring biotin, and also to provide a modified biotin which shows a high affinity to such streptavidin mutant reduced in affinity to the naturally-occurring biotin. It is a further object of this invention to provide a diagnostic/therapeutic drug based on combination of the streptavidin mutant and the modified biotin, and a diagnostic/therapeutic kit based on combination of the streptavidin mutant and the modified biotin.
After thorough investigations aimed at solving the problems above, the present inventors succeeded in obtaining a streptavidin mutant having a reduced affinity to the naturally-occurring biotin, by further introducing predetermined amino acid mutations into the low-immunogenic streptavidin mutant having been described in International Patent WO2010/095455. The present inventors concurrently synthesized a dimeric compound of modified biotin by partially modifying the biotin structure. The present inventors then examined affinity between the streptavidin mutant and the dimeric compound of modified biotin, and found out combinations thereof having high-affinity. The findings led us to work out this invention.
[1] A compound represented by Formula (1) below:
##STR00001##
(in Formula, each of X1a, X1b, X2a and X2b independently represents O or NH, each of Y1 and Y2 independently represents C or S, each of Z1 and Z2 independently represents O, S or NH, each of V1 and V2 independently represents S or S+—O−, each of n1 and n2 independently represents 0 or 1, each of m1 and m2 independently represents an integer from 1 to 10, and L represents a linking group.)
[2] The compound of [1], wherein both of n1 and n2 represent 0, and being represented by Formula (2) below:
##STR00002##
(in Formula, X1a, X1b, X2a, X2b, Y1, Y2, Z1, Z2, V1, V2, m1, m2 and L are synonymous to those in Claim 1).
[3] The compound of [1] or [2], wherein L represents —CONH—, —NHCO—, —O—, alkylene group having 1 to 10 carbon atoms, optionally substituted phenylene group, or any of combinations of them.
[4] The compound of any one of [1] to [3], wherein L represents —CONH—(CH2)p—CONH—(CH2)q—O—(CH2)r—NHCO(CH2)s—NH—CO—, —CONH—(CH2)p—CONH—(CH2)q—NHCO—(CH2)s—NH—CO—, —CONH—(CH2)p—CONH-(optionally substituted phenylene group)-NHCO—(CH2)s—NH—CO—, —CONH—CH(COOCH3)—(CH2)p—NHCO-(optionally substituted phenylene group)-CONH—(CH2)s—CH(COOCH3)—NH—CO—, or —CONH—(CH2)p—O—(CH2)t—NHCO-(optionally substituted phenylene group)-CONH—(CH2)s—O—(CH2)u—NH—CO— (in Formulae, each of p, q, r, s, t and u independently represents an integer from 1 to 10).
[5] A compound represented by any one of Formulae below:
##STR00003##
##STR00004##
[6] A compound comprising the compound of any one of [1] to [5], bound with a chelate group capable of capturing a radioisotope.
[7] A compound comprising the compound of any one of [1] to [5], bound with a fluorescent compound or a drug compound.
[8] A compound represented by any one of formulae below:
##STR00005##
##STR00006##
[9] A streptavidin mutant comprising an amino acid sequence in which Asn at amino acid residue 37 in the amino acid sequence represented by SEQ ID NO: 3 is substituted with other amino acid residue.
[10] A streptavidin mutant comprising an amino acid sequence represented by SEQ ID NO: 4.
[11] A DNA encoding the streptavidin mutant described in [9] or [10].
[12] A streptavidin mutant-molecular probe conjugate, obtained by combining the streptavidin mutant described in [9] or [10] with a molecular probe.
[13] The streptavidin mutant-molecular probe conjugate of [12], wherein the molecular probe is an anti-human CD20 antibody.
[14] The streptavidin mutant-molecular probe conjugate of [12], wherein the molecular probe is rituximab.
[15] The streptavidin mutant-molecular probe conjugate of [12], wherein the molecular probe is an anti-epiregulin single chain antibody.
[16] A therapeutic agent, or in vivo or in vitro diagnostic agent, comprising the streptavidin mutant-molecular probe conjugate described in any one of [12] to [15].
[17] A therapeutic, or in vivo or in vitro diagnostic kit, comprising (a) the streptavidin mutant-molecular probe conjugate described in any one of [12] to [15]; and (b) an in vivo or in vitro diagnostic substance, or a therapeutic substance, labeled with the compound described in any one of [1] to [5].
According to this invention, there is provided a combination of the streptavidin mutant having a reduced immunogenicity and a reduced affinity to the naturally-occurring biotin, and a dimeric compound of modified biotin having a high affinity to such streptavidin mutant. The combination of the streptavidin mutant and the dimeric compound of modified biotin of this invention is useful in diagnostic/therapeutic processes based on the pretargeting method.
This invention will further be detailed below.
(1) Dimeric Compound of Modified Biotin
A dimeric compound of modified biotin of this invention is a compound represented by formula (1) below, and preferably a compound represented by formula (2) where n1 and n2 in formula (1) represent 0.
##STR00007##
(in Formulae, each of X1a, X1b, X2a and X2b independently represents 0 or NH, each of Y1 and Y2 independently represents C or S, each of Z1 and Z2 independently represents 0, S or NH, each of V1 and V2 independently represents S or S+—O−, each of n1 and n2 independently represents an integer of 0 or 1, each of m1 and m2 independently represents integer from 1 to 10, and L represents a linking group.)
In formula (1) and formula (2), portions represented by the structures below:
##STR00008##
are preferably any one of; but not limited to, the structures below:
##STR00009##
Each of m1 and m2 represents an integer from 1 to 10, preferably from 2 to 10, more preferably from 2 to 8, and even more preferably from 2 to 6.
L preferably represents —CONH—, —NHCO—, —O—, alkylene group having 1 to 10 carbon atoms, optionally substituted phenylene group, or linking group composed of combination thereof. L more preferably represents —CONH—(CH2)p—CONH—(CH2)q—O—(CH2)r—NHCO—(CH2)s—NH—CO—, —CONH—(CH2)p—CONH—(CH2)q—NHCO—(CH2)s—NH—CO—, —CONH—(CH2)p—CONH-(optionally substituted phenylene group)-NHCO—(CH2)s—NH—CO—, —CONH—CH(COOCH3)—(CH2)p—NHCO-(optionally substituted phenylene group)-CONH—(CH2)s—CH(COOCH3)—NH—CO—, or —CONH—(CH2)p—O—(CH2)r—NHCO-(optionally substituted phenylene group)-CONH—(CH2)s—O—(CH2)u—NH—CO— (in the formulae, each of p, q, r, s, t, and u independently represents an integer of 1 to 10). More preferably, each of p, q, r and s independently represents an integer of 2 to 8, and even more preferably an integer of 2 to 6. Even more preferably, each oft and u independently represents an integer of 1 to 4. Substituent on the phenylene group is exemplified by —COOH, —CONH2, optionally substituted amido group, and —CO—NH2.
The compounds represented by formula (1) or formula (2) of this invention may be synthesized by the methods described later in Example 1. Compounds 5, 7, 11, 13, 15, 22, 24, 36 and 50 in Example 1 are the compounds represented by formula (1) or formula (2) of this invention.
Method of Synthesizing Compound 5
To an ethyl acetate solution of Compound 1, are added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and N,N-dimethylformamide. The mixture is added with 2,2′-oxybis(ethylamine) preliminarily dissolved in a mixed solvent of chloroform and N,N-dimethylformamide, and the mixture is allowed to react at room temperature, to obtain tert-butyl 6,6′-[2,2′-oxybis(ethane-2,1-diyl)bis(azanediyl)]bis(6-oxohexane-6,1-diyl)dicarbonate (Compound 2). To a dichloromethane solution of dicarbamate Compound 2, trifluoroacetic acid is added, and the mixture is allowed to react at room temperature for 30 minutes, to obtain N,N′-[2,2′-oxybis(ethane-2,1-diyl)]bis(6-aminohexanamido) (Compound 3). To a mixed solvent of N,N-dimethylformamide and pyridine containing diamine 3, EZ-Link® NHS-Iminobiotin is added, and the mixture is allowed to react at room temperature. The crude product is dissolved into a mixed solvent of dioxane and water, added with a 25% aqueous ammonia solution, and the mixture is allowed to react at room temperature, to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-(5,12,20,27-tetraoxo-16-oxa-6,13,19,26-tetraazahentriacontane-1,3H-diyl)bis[tetrahydro-1H-thieno[3,4-d]imidazole-2(3H)-iminium] di(2,2,2-trifluoroacetate) (Compound 5).
Method of Synthesizing Compound 7
To a mixed solvent of N,N-dimethylformamide and pyridine containing diamine 6, EZ-Link® NHS-Iminobiotin is added, and the mixture is allowed to react at room temperature. After the solvent is evaporated off under reduced pressure, the residue is dissolved in dioxane, added with 25% aqueous ammonia, and the mixture is allowed to react at room temperature, to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-(5,12,18,25-tetraoxo-6,13,17,24-tetraazanonacosane-1,29-diyl)bis[tetrahydro-1H-thieno[3,4-d]imidazole-2(3H)-iminium] di(2,2,2-trifluoroacetate) (Compound 7).
Method of Synthesizing Compound 11
To an N,N-dimethylformamide solution of Compound 1, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride is added, then ethyl 3,5-diaminobenzoate (Compound 8) dissolved in N,N-dimethylformamide is added, and the mixture is allowed to react at room temperature, to obtain ethyl 3,5-bis[6-(tert-butoxycarbonylamino)hexanamido]benzoate (Compound 9). To a dioxane solution of dicarbamate Compound 9, a 4-N hydrogen chloride solution in dioxane is added, and the mixture is allowed to react at room temperature, to obtain 6,6′-[5-(ethoxycarbonyl)-1,3-phenylene]bis(azanediyl)bis(6-oxohexane-1-ammonium) dichloride (Compound 10). The ammonium salt 10 is added with N,N-dimethylformamide, and then with triethylamine for solubilization. The mixture is then added with EZ-Link® NHS-Iminobiotin, and allowed to react at room temperature. The crude product is dissolved into methanol, added with a 2-N aqueous sodium hydroxide solution, and the mixture is stirred at room temperature for 22 hours, to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-{5,5′-[6,6′-(5-carboxy-1,3-phenylene)bis(azanediyl)bis(6-oxohexane-6,1-diyl)]bis(azanediyl)bis(5-oxopentane-5,1-diyl)}bis(tetrahydro-1H-thieno[3,4-d]imidazole-2(3)-iminium) di(2,2,2-trifluoroacetate) (Compound 11).
Method of Synthesizing Compound 13
To a N,N-dimethylformamide solution of bisiminobiotin 11, added are N,N′-diisopropylcarbodiimide and 1-hydroxybenzotriazole monohydrate, further added is an N,N-dimethylformamide solution of amine 12, and the mixture is allowed to react at 60° C., to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-{5,5′-[6,6′-(5-(2-(2-(2-aminoethoxy)ethoxy)ethylcarbonyl)-1,3-phenylene)bis(azanediyl)bis(6-oxohexane-6,1-diyl)]bis(azanediyl)bis(5-oxopentane-5,1-diyl)}bis(tetrahydro-1H-thieno [3,4-d]imidazole-2(3H)-iminium) tri(2,2,2-trifluoroacetate) (Compound 13).
Method of Synthesizing Compound 15
Diamine 10 is added with dioxane and pyridine, further with EZ-Link® NHS-Iminobiotin, and the mixture is allowed to react at room temperature. The solvent is evaporated off under reduced pressure, the crude product is dissolved in dioxane and water, added with 28% aqueous ammonium, and the mixture is allowed to react at room temperature, to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-{5,5′-[6,6′-(5-carbamoyl-1,3-phenylene)bis(azanediyl)bis(6-oxohexane-6,1-diyl)]bis(azanediyl)bis(5-oxopentane-5,1-diyl)}bis[tetrahydro-1H-thieno[3,4-d]imidazole-2(3H)-iminium]di(2,2,2-trifluoroacetate) (Compound 15).
Method of Synthesizing Compound 22
To an N,N-dimethylformamide solution of 5-(4-iodobenzamido)isophthalic acid, added are 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and 1-hydroxybenzotriazole monohydrate, further added is an N,N-dimethylformamide solution of amine 12, and the mixture is allowed to react at room temperature, to obtain N1,N3-bis{2-[2-(2-(tert-butoxycarbonylamino)ethoxy)ethoxy]ethyl}-5-(4-iodobenzamido)isophthalamide (Compound 17).
To a dichloromethane solution of dicarbamate Compound 17, trifluoroacetic acid is added, and the mixture is allowed to react at room temperature, to obtain N1,N3-bis{2-[2-(2-aminoethoxy)ethoxy]ethyl}-5-(4-iodobenzamido)isophthalamide (Compound 18).
To a N,N-dimethylformamide solution containing Boc-Asp(OtBu)—OH (Compound 19a) and N-hydroxysuccinimide, added is 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, and the mixture is allowed to react at room temperature, to obtain (S)-1-tert-butyl 4-(2,5-dioxopyrrolidine-1-yl) 2-(tert-butoxycarbonylamino)succinate (Compound 19).
To a mixed solvent of dioxane and pyridine containing diamine Compound 18, activated ester 19 is added, the mixture is allowed to react at room temperature, Compound 19 is further added, and the mixture is allowed to react at room temperature, to obtain tert-butyl (14S,14′S)-1,1′-[5-(4-iodobenzamido)-1,3-phenylene]bis[4-(tert-butoxycarbonylamino)-1,12-dioxo-5,8-dioxa-2,11-diazapentadecanoate] (Compound 20).
Compound 20 is added with trifluoroacetic acid, and the mixture is allowed to react at room temperature, to obtain (14S,14′S)-1,1′-[5-(4-iodobenzamido)-1,3-phenylene]bis(14-carboxy-1,12-dioxo-5,8-dioxa-2,11-diazatetradecane-14-ammonium) di(2,2,2-trifluoroacetate) (Compound 21).
Bisamino acid 21 is suspended into a mixed solvent of dioxane and water, a 1-N aqueous sodium hydroxide solution is added, the mixture is stirred at room temperature for solubilization, added with EZ-Link® NHS-Iminobiotin, and is allowed to react at room temperature. A 2-N aqueous sodium hydroxide solution is added, and the mixture is further allowed to react at room temperature, to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-{(14S,4′S)-1,1′-[5-(4-iodobenzamido)-1,3-phenylene]bis(14-carboxy-1,12,16-trioxo-5,8-dioxa-2,11,15-triazaeicosane-20,1-diyl)}bis(tetrahydro-1H-thieno[3,4-d]imidazole-2(3H)-iminium) di(2,2,2-trifluoroacetate) (Compound 22).
Method of Synthesizing Compound 24
To an N,N-dimethylformamide solution of diamine 3, biotin N-hydroxysuccinimide ester (Compound 23) is added, and the mixture is allowed to react at room temperature, to obtain N,N′-[2,2′-oxybis(ethane-2,1-diyl)]bis{6-[5-((3a,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazole-4-yl)pentanamido]hexanamide} (Compound 24).
Method of Synthesizing Compound 36
2-Iminobiotin 39 is added with trifluoroacetic acid, the mixture is stirred, and an excessive portion of trifluoroacetic acid is removed by evaporation under reduced pressure. To an acetonitrile solution of the obtained white solid, added are pyridine and disuccinimide 40, and the mixture is stirred at 30° C. After the solvent is evaporated off under reduced pressure, the residue is dried in vacuo, to obtain Compound 41. To a mixed solvent of N,N-dimethylformamide and triethylamine containing diamine 34 is added ester 41 prepared from 2-iminobiotin 39, the mixture is stirred at room temperature, the solvent is evaporated off under reduced pressure, the obtained crude product is purified by reversed-phase silica gel column chromatography (water/methanol=2:1→1:2), to obtain Compound 35. To an aqueous solution of bisiminobiotin 35, trifluoroacetic acid is added, the mixture is stirred at 50° C. for 4 hours, the solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase silica gel column chromatography (water/methanol=2:1→1:2), to obtain Compound 36.
Method of Synthesizing Compound 50
To an N,N-dimethylformamide solution of disuccinimide compound 30, added is an N,N-dimethylformamide solution of amine 45, and the mixture is stirred at room temperature. An additional N,N-dimethylformamide solution of amine 45 is added, and the mixture is stirred at room temperature. After the solvent is evaporated off under reduced pressure, the residue is added with ethyl acetate, washed successively with 1-M aqueous sodium hydroxide solution, 1-M hydrochloric acid, and a saturated sodium chloride solution, the organic layer is dried over sodium sulfate, the solvent is evaporated off under reduced pressure, the obtained crude product is purified by silica gel column chromatography (dichloromethane/hexane=1:30→1:20→1:10→1:5), to obtain Compound 46. An aqueous solution of dicarbamate Compound 47 obtained above is added with trifluoroacetic acid under cooling on ice, stirred, heated to room temperature, and further stirred. After the solvent is evaporated off under reduced pressure, the residue is dried in vacuo, to obtain a crude product containing Compound 48. To a test tube containing Compound 41 prepared from 2-iminobiotin 39 are added an N,N-dimethylfomamide solution of diamine 48 and diisopropylethylamine, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase silica gel column chromatography (methanol/water=2:1, 0.3% TFA), to obtain Compound 49. Bisiminobiotin 49 is then added with a mixed solvent of trifluoroacetic acid and water, the mixture is heated to 50° C. and stirred. After the solvent is evaporated off under reduced pressure, the residue is dried in vacuo, to obtain Compound 50.
According to this invention, there is also provided a compound composed of a dimeric compound of modified biotin of this invention, bound with a chelate group capable of capturing a radioisotope. The chelete group usable in this invention includes DOTA (1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraacetate), DTPA (diethylenetriamine pentaacetate), TETA (1,4,8,11-tetraazacyclotetradecane-N, N′, N″, N′″-tetraacetate), N2S2, MAG3 and CHX-A-DTPA.
According to this invention, there is also provided a compound composed of the above-described compound bound with a chelete group, and a radioisotope captured thereon. Among the radioisotopes possibly captured by the chelete group, those available for imaging include gamma-ray emitting nuclides (67Ga, 99mTc, 111In, 123I) and positron emitting nuclides (18F, 62Cu, 64Cu, 66Ga, 68Ga, 76Br, 86Y, 89Zr, 4Tc, 124I). Those suitably used as therapeutic radioisotope include beta-ray emitting nuclides (32P, 67Cu, 89Sr, 90Y, 114mIn, 117mSn, 131I, 153Sm, 166Ho, 177Lu, 186Re, 188Re, etc.), alpha-ray emitting nuclides (211At, 212Bi, 212Pb, 213Bi, 223Ra, 225Ac, etc.) and Auger electron emitting nuclides (125I, 165Er, etc.). Among these nuclides, 64Cu, 124I, 76Br, 68Ga, 99mTc, 123I, 131I and 90Y are preferably used.
According to this invention, there is also provided a compound composed of the above-described dimeric compound of modified biotin of this invention bound with a fluorescent compound or drug compound (e.g., anticancer drug).
The fluorescent compound suitably used in this invention is exemplified by fluorescein-5-isothiocyanate (FITC), IRDye (registered trademark) 800, and fluorescein. The drug (e.g., anticancer drug) suitably used in this invention is exemplified by PBD (pyrrolobenzodiazepin) class (e.g., SJG-136, SG2202, etc.), maytansine analogues (e.g., DM1, DM4, etc.), dolastatin analogues (e.g., monomethyl auristatin E (MMAE), monomethyl auristatin F (MMAF), dolastatin 10, tubulysin, etc.), duocarmycin analogues (e.g., DC1, DC4, DC44, etc.), camptothecin analogues (e.g., SN-38 etc.), and others (e.g., methotrexate, vinblastine, calicheamicin, α-amanitin, doxorubicin, and melphalan).
Specific examples of the compound composed of the compound represented by formula (1) or formula (2) of this invention bound with a chelate group capable of capturing a radioisotope, and the compound composed of the compound represented by formula (1) or formula (2) of this invention bound with a fluorescent compound or a drug compound, are exemplified by Compounds 14, 42, 44, 51, 52 and 59 in Example 1, which may be synthesized according to the synthetic methods described later in Example 1.
Method of Synthesizing Compound 14
A methanol solution of bisiminobiotin 13 is added with triethylamine and fluorescein-5-isothiocyanate, and the mixture is allowed to react at room temperature, to obtain (3aS,3a′S,4S,4′S,6aR,6a′R)-4,4′-{5,5′-[6,6′-(5-(2-(2-(2-(3-(3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-yl)thioureido)ethoxy)ethoxy)ethylcarbamoyl)-1,3-phenylene)bis(azanediyl)bis(6-oxohexane-6,1-diyl)]bis(azanediyl)bis(5-oxopentane-5,1-diyl)}bis(tetrahydro-1H-thieno[3,4-d]imidazole-2(3H)-iminium) di(2,2,2-trifluoroacetate) (Compound 14).
Method of Synthesizing Compound 42
To a mixed solvent of methanol and triethylamine containing bisiminobiotin 36, DOTA-NHS-ester 37 was added, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% HCOOH in MQ, ramp time=40 min (17.5-57.5%), tr=31.5 min), to obtain Compound 42.
Method of Synthesizing Compound 44
To a mixed solvent of N,N-dimethylformamide and triethylamine containing bisiminobiotin 36, IRDye® 800CW NHS Ester is added, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% TFA in MQ, ramp time=40 min (17.5-57.5%), tr=40.9 min), to obtain Compound 44.
Method of Synthesizing Compound 51
To a mixed solvent of methanol and triethylamine containing bisiminobiotin 50, DOTA-NHS-ester 37 is added, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% TFA in MQ, ramp time=40 min (17.5-57.5%), tr=32.6 min), to obtain Compound 51.
Method of Synthesizing Compound 52
To a mixed solvent of methanol and triethylamine containing bisiminobiotin 50, 5(6)-carboxyfluorescein N-hydroxysuccinimide ester 51 is added, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, the obtained crude product is purified by reversed-phase column chromatography (methanol/water=1:1→2:1, 0.5% TEA), and further purified through Sephadex 20LH (methanol, 1% TFA), to obtain Compound 52.
Method of Synthesizing Compound 59
To a dichloromethane solution containing SN38 Boc-protected compound 53 and Cbz-Ala-OH 54 is added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and dimethylaminopyridine under cooling on ice, the mixture is gradually heated to room temperature, and stirred. The mixture is added with dichloromethane, washed successively with an aqueous sodium hydrogen carbonate solution, water, 0.1-M hydrochloric acid, and a saturated sodium chloride solution, the organic layer is dried over sodium sulfate, the solvent is evaporated off under reduced pressure, and the obtained crude product is purified by silica gel column chromatography (dichloromethane/methanol=30:1), to obtain Compound 55. To an ethyl acetate solution of Compound 55, Pd/C is added, the atmosphere in the reaction vessel is replaced with hydrogen, the mixture is stirred at room temperature, then stirred at 40° C., and filtered through celite. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by thin layer chromatography (dichloromethane/methanol=30:1), to obtain Compound 56. To a dichloromethane solution of Compound 56, triphosgene and pyridine are added under cooling on ice, the mixture is heated to room temperature and stirred. After the solvent is evaporated off under reduced pressure, the residue is dried in vacuo, to obtain a crude product (brown liquid) containing Compound 57. To a methanol solution of crude product containing bisiminobiotin 50 and Compound 57, triethylamine is added, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase thin layer chromatography (methanol/water=3:1, 1% TFA), to obtain Compound 58. To an aqueous solution of bisiminobiotin 58, trifluoroacetic acid is added, and the mixture is stirred at room temperature. The solvent is evaporated off under reduced pressure, and the obtained crude product is purified by reversed-phase thin layer chromatography (methanol/water=3:1, 1% TFA), to obtain Compound 59.
(2) Streptavidin Mutant
The streptavidin mutant characteristically contains mutation of predetermined amino acids in the amino acid sequence of the core streptavidin represented by SEQ ID NO: 2, and is reduced in immunogenicity as compared with the wild-type streptavidin, and is also reduced in affinity to the naturally-occurring biotin or biocytin.
The amino acid sequence of wild-type (native) core streptavidin is represented by SEQ TD NO: 2 in the Sequence Listing, and the nucleotide sequence encoding it is represented by SEQ ID NO: 1 in the sequence listing.
The streptavidin mutant of this invention is specifically exemplified by a streptavidin mutant composed of an amino acid sequence in which, in the amino acid sequence represented by SEQ ID NO: 3, Asn at the 37th amino acid residue is substituted with other amino acid residue. It is more preferably a streptavidin mutant containing the amino acid sequence represented by SEQ ID NO: 4.
The amino acid sequence represented by SEQ ID NO: 3 has the mutations listed below in streptavidin whose amino acid sequence is represented by SEQ ID NO: 2:
(1) mutation given by substitution of tyrosine at position 10 with serine;
(2) mutation given by substitution of tyrosine at position 71 with serine;
(3) mutation given by substitution of arginine at position 72 with lysine;
(4) mutation given by substitution of glutamic acid at position 89 with aspartic acid;
(5) mutation given by substitution of arginine at position 91 with substituted with lysine;
(6) mutation given by substitution of glutamic acid at position 104 with asparagine;
(7) mutation given by substitution of asparagine at position 11 with aspartic acid;
(8) mutation given by substitution of serine at position 15 with aspartic acid; and
(9) mutation given by substitution of serine at position 33 with asparagine.
The amino acid sequence represented by SEQ ID NO: 4 additionally contains the mutation below, in the amino acid sequence represented by SEQ ID NO: 3:
(10) mutation given by substation of asparagine at position 37 with glycine:
In this invention, the phrase stating that “ . . . is reduced in immunogenicity as compared with the wild-type streptavidin” means that the immunogenicity is reduced when the streptavidin mutant was administered to mammals including human. Reduction in immunogenicity may be confirmed typically by the method below. That is, the streptavidin mutant of this invention is analyzed to find how it is reactive with an anti-streptavidin antiserum obtained from a crab-eating monkey immunized with wild-type streptavidin, and reduction in immunogenicity, from the level shown by the wild-type streptavidin, is determined if the reactivity to the anti-streptavidin antiserum is found to be decreased from that of the wild-type streptavidin. According to the way of determining such reduction in immunogenicity, the immunogenicity of the streptavidin mutant of this invention is decreased preferably down to 80% or below, more preferably 60% or below, more preferably 20% or below, even more preferably 15% or below, yet more preferably 10% or below, and particularly 5% or below, of the level shown by the wild-type streptavidin.
In this invention, the phrase stating that “ . . . is reduced in affinity to the naturally-occurring biotin or biocytin” means that binding potential of the streptavidin mutant with the naturally-occurring biotin or biocytin is lowered from the binding potential of streptavidin with the naturally-occurring biotin or biocytin. Affinity/binding potential of the streptavidin mutant with the naturally-occurring biotin or biocytin may be evaluated typically by SPR analysis. Affinity of the streptavidin mutant of this invention with the naturally-occurring biotin or biocytin has been decreased preferably down to 80% or below, more preferably 70% or below, more preferably 60% or below, even more preferably 50% or below, and yet more preferably 40% or below, of the level shown by the wild-type streptavidin.
According to this invention, there is also provided a DNA encoding the streptavidin mutant of this invention. The DNA of this invention may be produced by site-directed mutagenesis of DNA encoding the wild-type (native) streptavidin.
The DNA encoding the streptavidin mutant of this invention may be used after being introduced into a vector. In particular, the streptavidin mutant of this invention may be produced by introducing the DNA encoding the streptavidin mutant of this invention into an expression vector, and then transforming a host with the expression vector, so as to express the streptavidin mutant of this invention.
When E. coli is used as a host, the vector used in this invention preferably has a replication origin (ori), and also has a gene for selecting the transformed host (e.g., drug-resistance gene resistant to drugs including ampicillin, tetracycline, kanamycin or chloramphenicol, etc.). The expression vector preferably has a promoter capable of efficiently expressing the streptavidin mutant of this invention in the host, such as lacZ promoter or T7 promoter Examples of such vector include M13 vector, pUC vector, pBR322, pBluescript, pCR-Script, pGEX-5X-1 (Pharmacia), “QIAexpress system” (QIAGEN), pEGFP, and pET (in this case, BL21 having T7 RNApolymeraze expressed therein is preferably used as a host). The vector may also be attached with a signal sequence or the like, so as to increase the yield of the streptavidin mutant of this invention.
The vector may be introduced into the host cell typically by the calcium chloride method or electroporation. The vector may also be attached with a sequence capable of encoding a tag for improving solubility, such as glutathione-S-transferase, thioredoxin or maltose-binding protein. The vector may also be attached with a sequence capable of encoding atag designed for simplifying the purification, such as polyhistidine tag, Myc epitope, hemagglutinin (HA) epitope, T7 epitope, Xpress tag, FLAG peptide tag, or other known sequences.
Examples of the expression vector other than E. coli include mammal-derived expression vectors (e.g., pcDNA3 (Invitrogen), pEGF-BOS (Nucleic Acids. Res. 1990,18(17), p 5322), pEF, pCDM8); insect cell-derived expression vectors (e.g., “Bac-to-BAC baculovirus expression system” (from Gibco-BRL), pBacPAK8); plant-derived expression vectors (e.g., pMH1, pMH2); animal virus-derived expression vectors (e.g., pHSV, pMV, pAdexLew); retrovirus-derived expression vectors (e.g., pZIPneo); yeast-derived expression vectors (e.g., “Pichia Expression Kit” (Invitrogen), pNV11, SP-Q01); and hay bacillus (Bacillus subtilis)-derived expression vector (e.g., pPL608, pKTH50).
For the purpose of expression in an animal cell such as CHO cell, COS cell, NIH3T3 cell or the like, it is essential for the expression vector to have a promoter which is necessary for the expression in the cell, such as SV40 promoter (Mulligan et al., Nature (1979) 277, 108), MMLV-LTR promoter, EF1α promoter (Mizushima et al., Nucleic Acids Res. (1990) 18, 5322), or CMV promoter. The expression vector more preferably has a gene for selecting transformation of the cell (e.g., drug-resistance gene identifiable by drugs (neomycin, G418, etc.). Examples of such vector include pMAM, pDR2, pBK-RSV, pBK-CMV, pOPRSV and pOP13.
Host cell into which the vector is introduced may be either prokaryotes or eukaryotes, without special limitation. For example, E. coli and various types of animal cells may be used.
As the eukaryotic cells, for example, animal cell, plant cell, or fungal cell may be used as the host. Animal cell suitably used herein include mammalian cells such as CHO cell, COS cell, 3T3 cell, HeLa cell and Vero cell; and insect cells such as Sf9, Sf21 and Tn5. For the purpose of mass expression in the animal cell, CHO cell is particularly preferable. The vector may be introduced into the host cell typically by calcium phosphate method, DEAE dextran method, a method using cationic ribosome DOTAP (from Boehringer Mannheim), electroporation method, lipofection or the like.
As for the plant cells, a well known example of protein-producing system is Nicotiana tabacum-derived cell, which may be cultured using callus. Known examples of fungal cell include those of yeast fungi, including genus Saccharomyces, represented by Saccharomyces cerevisiae; and filamentous fungus including genus Aspergillus, represented by Aspergillus niger.
As the procaryotic cells suitably used herein, exemplified are Escherichia coli (E. coli), such as JM109, DH5α and HB101; and hay bacillus (Bacillus subtilis).
The streptavidin mutant of this invention may be obtained by transforming these cells using the DNA of this invention, and by culturing the transformed cells in vitro. The cells may be cultured by any of known methods. For example, DMEM, MEM, RPMI1640 or IMDM may be used as a culture medium for the animal cells. The culture in this case may be allowed to proceed in the presence of serum such as fetal calf serum (FCS), or may be in accordance with serum-flee culture. The culture is preferably allowed to proceed at pH6 to 8 or around. The culture is typically allowed to proceed at approximately 30 to 40° C. for approximately 15 to 200 hours, with optional replacement of medium, ventilation and stirring. Also a growth factor may be added in order to promote the growth of the cells.
(3) Use of Streptavidin Mutant and Modified Biotin
According to this invention, there is also provided a streptavidin mutant-molecular probe conjugate, obtained by combining the streptavidin mutant of this invention with a molecular probe; and a therapeutic agent or diagnostic agent containing the streptavidin mutant-molecular probe conjugate. Moreover, the streptavidin mutant-molecular probe conjugate may be provided as a therapeutic or diagnostic kit, after combining it with a diagnostic or therapeutic substance labeled with the modified biotin which shows affinity to the streptavidin mutant of this invention. The molecular probe suitably used herein is exemplified by antibody, peptide, nucleic acid, and aptamer, and more specifically, by antibody, peptide, nucleic acid and aptamer which are targeted at antigens specifically expressed in cancer, the antigen includes:
epiregulin, ROBO1,2,3,4, 1-40-β-amyloid, 4-1BB, 5AC, 5T4, ACVR2B, adenocarcinoma antibody, α-fetoprotein, angiopoietin2, anthrax toxin, AOC3 (VAP-1), B-lymphoma cell, B7-H3, BAFF, β amyloid, C242 antibody, C5, CA-125, carbonic anhydraze 9 (CA-IX), cardiac myosin, CCL11 (eotaxin-1), CCR4, CCR5, CD11, CD18, CD125, CD140a, CD147 (basigin), CD147 (basigin), CD15, CD152, CD154 (CD40L), CD154, CD19, CD2, CD20, CD200, CD22, CD221, CD23 (IgE receptor), CD25 (α chain of IL-2 receptor), CD28, CD3, CD30 (TNFRSF8), CD33, CD37, CD38 (cyclic ADP ribose hydrolase), CD4, CD40, CD41 (integrin α-IIib), CD44 v6, CD5, CD51, CD52, CD56, CD6, CD70, CD74, CD79B, CD80, CEA, CFD, ch4D5, CLDN18.2, Clostridium difficile, clumping factor A, CSF2, CTLA-4, cytomegalovirus, cytomegalovirusglycoprotein B, DLL4, DR5, E. coli Shiga Toxin 1, E. coli Shiga Toxin 2, EGFL7, EGFR, endotoxin, EpCAM, episialin, ERBB3, Escherichia coli, F (fusion) protein of respiratory syncytial virus, FAP, fibrin IIβ chain, fibronectin extra domain-B, folic acid receptor 1, Frizzled receptor, GD2, GD3 ganglioside, GMCSF receptor a chain, GPNMB, hepatitis B surface antigen, hepatitis B virus, HER1, HER2/neu, HER3, HGF, HIV-1, HLA-DRβ, HNGF, Hsp90, human β amyloid, human scatter factor receptor kinase, human TNF, ICAM-1 (CD54), IFN-α, IFN-γ, IgE, IgE Fc region, IGF-1 receptor, IGF-I, IgG4, IGHE, IL-1β, IL-12, IL-13, IL-17, IL-17A, IL-22, IL-23, IL-4, IL-5, IL-6, IL-6 receptor, IL-9, ILGF2, influenza A hemagglutinin, insulin-like growth factor I receptor, integrin α4, integrin α4β7, integrin α5β1, integrin α7β7, integrin αIIbβ3, integrin αvβ3, integrin γ derived protein, interferon receptor, interferon α/β receptor, ITGA2, ITGB2 (CD18), KIR2D, L-selectin(CD62L), Lewis-Y antigen, LFA-1 (CD11a), lipoteichoic acid, LOXL2, LTA, MCP-1, mesothelin, MS4A1, MUC1, mucin CanAg, myostatin, N-glycolylneuraminic acid, NARP-1, NCA-90 (granulocyte antigen), NGF, NOGO-A, NRP1, Oryctolagus cuniculus, OX-40, oxLDL, PCSK9, PD-1, PDCD1, PDGF-R α, phosphatidylserine, prostate cancer cell, Pseudomonas aeruginosa, rabies virus glycoprotein, RANKL, respiratory syncytial virus, RHD, Rh (Rhesus) factor, RON, RTN4, sclerostin, SDC1, selectin P, SLAMF7, SOST, sphingosine-1-phosphate, TAG-72, TEM1, tenascin C, TFPI, TGFβ1, TGFβ2, TGF-β, TNF-α, TRAIL-R1, TRAIL-R2, tumor antigen CTAA16.88, tumor-specific glycosilation of MUC1, TWEAK receptor, TYRP1 (glycoprotein 75), VEGF-A, VEGFR-1, VEGFR2, vimentin, VWF
Preferable examples of the molecular probe include anti-human CD20 antibody (e.g., Rituximab), and anti-epiregulin single chain antibody.
Rituximab is an anti-human CD20 antibody, where human CD20 is expressed only in B cell. A therapeutic drug for B cell non-Hodgkin's lymphoma and mantle cell lymphona, obtained by isotopic labeling of murine anti-CD20 monoclonal antibody with 90Y, is commercially available under the registered trademark of “Zevalin”. This drug has an RI label directly bound to the anti-CD20 antibody, and needs several days after in vivo administration up to tumor accumulation, with an anxiety of serious side effect such as bone-marrow suppression induced by RI. As a solution to these problems, the pre-targeting method has been proposed (Non-Patent Literature 3). Pagneli et al. has investigated into the pre-targeting method using a fusion protein of anti-CD20 antibody-scFv and a streptavidin mutant, and RI-labeled biotin or bisbiotin (Non-Patent Literature 5).
Epiregulin is a member of epidermal growth factor, and is known to function as a cancer growth inhibitor capable of inducing changes in cytomorphology of HeLa cell. Aburatani et al. have produced an anti-epiregulin antibody (WO2008/047723). Lee et al. has humanized and evaluated an anti-epiregulin antibody (Biochemical and Biophysical Research communications, 444(2013), 1011-1017).
According to this invention, the streptavidin mutant of this invention may specifically be accumulated to cancer cell, by preparing a fused body of a molecular probe such as a cancer antigen-specific antibody molecule with the streptavidin mutant of this invention, and by administering it to a patient. Then by administering a diagnostic or therapeutic substance bound with the modified biotin which shows affinity to the streptavidin mutant (fluorescent dye, chemoluminescence agent, radioisotope, sensitizer composed of metal compound or the like, neutron capturing agent composed of metal compound or the like, low molecular weight compound such as drug, micro or nanobubble, protein, etc.) to a patient, the substance may specifically be accumulated to the cancer cell. In this invention, antibody production may be suppressed as a result of reduction in immunogenicity, and thereby it now becomes possible to avoid early in vivo clearance of the mutant streptavidin due to antibody, and a shock such as anaphylaxis. According to this invention, by using the streptavidin combined with patient's tissue, serum or the like as an in vitro diagnostic drug or a clinical reagent, the noise assignable to biotin or biotin-binding protein contained in the tissue, serum or the like, may be reduced, and this enables diagnosis or examination with higher S/N.
Alternatively, in this invention, a fused body of a molecular probe such as a cancer antigen-specific antibody molecule with the streptavidin mutant of this invention may be combined with a diagnostic or therapeutic substance bound with the modified biotin which shows affinity to the streptavidin mutant (fluorescent dye, chemoluminescence agent, radioisotope, sensitizer composed of metal compound or the like, neutron capturing agent composed of metal compound or the like, low molecular weight compound such as drug, micro or nanobubble, protein, etc.) to prepare a conjugate, and the obtained conjugate may be administered to a patient.
Various types of molecules may be used as the antibody to be bound to the streptavidin mutant. Either polyclonal antibody or monoclonal antibody may be used. IgG and in particular IgG1 is preferable, without special limitation on subclass of the antibody. The “antibody” herein includes all of modified antibodies and antibody fragments. Examples of the antibody include humanized antibody; human-type antibody; human antibody; antibodies derived from various animals including mouse, rabbit, rat, guinea pig and monkey; chimeric antibodies formed between human antibody and antibodies derived from various animals; diabody; scFv; Fd; Fab; Fab′; and F(ab)′2, but not limited thereto.
The conjugate of the streptavidin mutant and an antibody may be obtained by a method known to those skilled in the art. For example, the conjugate may be obtained by chemical binding (U.S. Pat. No. 5,608,060); or may be obtained in the form of fusion protein, by ligating a DNA encoding the streptavidin mutant and a DNA encoding the antibody, and then allowing it to be expressed in a host cell typically by using a vector. The DNA encoding the streptavidin mutant and the DNA encoding the antibody may be ligated via a DNA encoding an appropriate peptide, called linker. The streptavidin mutant-antibody conjugate is preferably produced, while maintaining the specific binding ability between the antibody and a target molecule.
This invention will further be detailed referring to Examples below, to which this invention is not limited.
General Method
Nuclear magnetic resonance (NMR) spectrum was measured using JEOL ECX500 (1H NMR: 500 MHz), or JEOL ECS400 (1H NMR: 400 MHz) spectrometer. Chemical shift was given in ppm, as a value away from an internal reference peak assignable to a residual solvent in a deuterated solvent (CDCl3: δ=7.26 ppm, CD3OD: δ=3.31 ppm). Low-resolution mass spectrum (LRMS) was measured using an ESI-MS system named Waters ZQ4000 spectrometer. Column chromatography was carried out using silica gel Merk 60 (230-400 mesh ASTM). The reactions were monitored by way of thin layer chromatography (TLC), or low-resolution mass spectrometry (LRMS).
Reversed-phase high performance liquid chromatography (HPLC) was carried out using JASCO-HPLC system. Ultraviolet radiation of 210 nm or 254 nm was used for detection, and a gradient solvent system (acetonitrile/0.1% trifluoroacetic acid in MQ) was used as the mobile phase. Analyses were carried out using YMC-Pack ODS-AM (150×4.6 mL) or YMC-Triart-C18 (150×4.6 mL) column, at a flow rate of 1 mL/min. Fractionation was carried out using YMC-Pack ODS-AM (250×20 mL) or YMC-Triart-C18 (250×10 mL) column, at a flow rate of 8 to 10 mL/min for the former, and at a flow rate of 3 mL/min for the latter.
EZ-Link (registered trademark) NHS-Iminobiotin was purchased from Thermo Fisher Scientific Inc. Other reagents were purchased from Aldrich, Tokyo Chemical Industry Co., Ltd. (TCI), Kanto Chemical Co., Inc. (Kanto), Wako Pure Chemical Industries, Ltd., and Watanabe Chemical Industries, Ltd. All reagents and solvents were used as sold, unless otherwise specifically noted.
##STR00010##
To an ethyl acetate (12 mL) solution of Compound 1 (1.40 g, 6.05 mmol) synthesized by a known method (Carlescu et al., Carbohydr. Res., (2010) 345, 33) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl, 1.22 g, 6.34 mmol) and N,N-dimethylformamide (6 mL), and the mixture was cooled on an ice bath. After adding 2,2′-oxybis(ethylamine) (0.30 g, 2.88 mmol) dissolved in a mixed solvent of chloroform (24 mL) and N,N-dimethylformamide (6 mL) to the reaction mixture, the mixture was stirred at room temperature for 17 hours. The mixture was then added with a saturated sodium chloride solution, the product was extracted into ethyl acetate, the organic layer was washed twice with a 0.5-N hydrochloric acid solution, then washed twice with an aqueous saturated sodium hydrogen carbonate solution, and further washed with a saturated sodium chloride solution. The organic layer was then dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol=20:1). Title Compound 2 (0.982 g, yield 64%, highly viscous yellow oil) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.29-1.36 (m, 4H), 1.43 (s, 18H), 1.48 (quint., 4H, J=7.5 Hz), 1.62 (quint., 4H, J=7.5 Hz), 2.20 (t, 4H, J=7.5 Hz), 3.02 (t, 4H, J=7.5 Hz), 3.35 (t, 4H, J=5.7 Hz), 3.51 (t, 4H, J=5.7 Hz); LRMS (ESI): m/z 553 [M+Na]+.
##STR00011##
To a dichloromethane (6 mL) solution containing dicarbamate Compound 2 (0.917 g, 1.73 mmol) was added trifluoroacetic acid (12 mL), and the mixture was stirred at room temperature for 30 minutes. After the solvent was evaporated off under reduced pressure, the residue was dissolved into methanol (1 mL), applied to Amberlite® IRA-400 column (basic resin, 20 mm×200 mm), and eluted with methanol. After the solvent was evaporated off under reduced pressure, the residue was dried in vacuo. Title Compound 3 (0.57 g, quant., pale yellowish white solid) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.35-1.40 (m, 4H), 1.53 (quint., 4H, J=7.5 Hz), 1.63 (quint., 4H, J=7.5 Hz), 2.22 (t, 4H, J=7.5 Hz), 2.70 (t, 4H, J=7.5 Hz), 3.35 (t, 4H, J=5.7 Hz), 3.51 (t, 4H, J=5.7 Hz);
LRMS (ESI): m/z 166 [M+2H]2+.
##STR00012##
To a solution of diamine 3 (7.0 mg, 0.0212 mmol) dissolved in a mixed solvent of N,N-dimethylformamide (0.4 mL) and pyridine (0.1 mL) was added EZ-Link® NHS-Iminobiotin (4, 18.4 mg, 0.0424 mmol), and the mixture was stirred at room temperature for 7 hours. After the solvent was evaporated off under reduced pressure, a mixed solvent (1:1) of acetone and diethyl ether was added to the residue, and sonicated. The deposited solid was collected by filtration, washed with the same solvent, and dried under reduced pressure. The crude product was dissolved into a mixed solvent of dioxane (1.2 mL) and water (0.8 mL), 25% aqueous ammonia (4.8 mL) was added, and the mixture was stirred at room temperature for 6 hours. The aqueous layer was washed with diethyl ether, and the solvent was evaporated off under reduced pressure. The obtained crude product was purified by reversed-phase HPLC (0-10-11-41-42-55 min; 0-0-22-52-100-100% CH3CN in 0.1% TFA in MQ, ramp time=30 min (22-52%), tr=22.0 min). Title Compound 5 (10.8 mg, two-step yield=65%, colorless amorphous matter) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.35 (quint., 4H, J=7.5 Hz), 1.46 (quint, 4H, J=7.5 Hz), 1.52 (quint., 4H, J=7.5 Hz), 1.55-1.72 (m, 10H), 1.78 (sext., 2H, J=7.5 Hz), 2.21 (t, 8H, J=7.5 Hz), 2.83 (d, 2H, J=13.2 Hz), 3.01 (dd, 2H, J=13.2, 5.2 Hz), 3.17 (t, 2H, J=7.5 Hz), 3.32 (ddd, 2H, J=10.3, 5.8, 4.6), 3.36 (t, 4H, J=5.2 Hz), 3.51 (t, 4H, J=5.2 Hz), 4.54 (dd, 2H, J=7.5, 4.6 Hz), 4.73 (dd, 2H, J=7.5, 5.2 Hz);
LRMS (ESI): m/z 391 [M+2H]2+.
##STR00013##
To a solution of diamine 6 (3.3 mg, 0.0115 mmol) synthesized by a known method and dissolved in a mixed solvent of N,N-dimethylformamide (0.4 mL) and pyridine (0.1 mL) was added EZ-Link® NHS-Iminobiotin (4, 10 mg, 0.0230 mmol), and the mixture was stirred at room temperature for 6 hours. After the solvent was evaporated off under reduced pressure, the residue was dissolved into dioxane (0.5 mL), 25% aqueous ammonia (2.0 mL) was added, and the mixture was stirred at room temperature for 6 hours. The aqueous layer was washed with diethyl ether, and the solvent was evaporated off under reduced pressure. The obtained crude product was purified by reversed-phase HPLC (YMC-Pack ODS-AM, gradient: 0-10-11-36-37-50 min; 0-0-17-42-100-100% CH3CN in 0.1% TFA in MQ, ramp time=25 min (17-42%), tr=26.7 min). Title Compound 7 (7.9 mg, two-stage yield=71%, colorless amorphous matter) was thus obtained.
1H NMR (400 MHz, CD3OD) δ: 1.31-1.38 (m, 4H), 1.42-1.55 (m, 8H), 1.56-1.70 (m, 10H), 1.78 (sext., 2H, J=8.0 Hz), 2.20 (q, 8H, J=7.2 Hz), 2.83 (d, 2H, J=13.4 Hz), 3.01 (dd, 2H, J=13.4, 4.5 Hz), 3.17 (t, 4H, J=8.0), 3.27 (s, 4H), 3.30-3.33 (m, 2H), 4.54 (dd, 2H, J=8.0, 4.5 Hz), 4.73 (dd, 2H, J=7.6 4.5 Hz);
LRMS (ESI): m/z 369 [M+2H]2+.
##STR00014##
To a solution of Compound 1 (2.82 g, 11.2 mmol) synthesized by a known method (Carlescu et al., Carbohydr. Res. (2010) 345, 33) and dissolved in N,N-dimethylformamide (25 mL) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl, 2.66 g, 12.8 mmol) and ethyl 3,5-diaminobenzoate 8 (0.96 g, 5.33 mmol) dissolved in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature for 2 hours. The mixture was added with a saturated sodium chloride solution and 1-N hydrochloric acid, the product was extracted into ethyl acetate, and the organic layer was washed twice with 0.5-N hydrochloric acid, then washed twice with an aqueous saturated sodium hydrogen carbonate solution, and further washed with a saturated sodium chloride solution. The organic layer was then dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate=1:1→1:3). Title Compound 9 (2.27 g, yield 59%, yellow oil) was thus obtained.
1H NMR (400 MHz, cdcl3) δ: 1.30-1.35 (m, 6H), 1.35-1.50 (m, 22H), 1.66 (quint., 4H, J=7.6 Hz), 2.31 (t, 4H, J=7.6 Hz), 3.05 (q, 4H, J=6.7 Hz), 4.30 (q, 4H, J=7.2 Hz), 4.76 (brs, 2H), 7.91 (s, 2H), 8.05 (s, 1H), 8.54 (s, 2H); LRMS (ESI): m/z 629 [M+Na]+.
##STR00015##
To a dioxane (20 mL) solution of dicarbamate compound 9 (2.27 g, 3.74 mmol) was added a 4-N hydrogen chloride solution in dioxane (20 mL), and the mixture was stirred at room temperature for 2 hours. The produced solid was washed with diethyl ether, and dried in vacuo. Ammonium salt 10 was quantitatively obtained. The solid was further dissolved into a small amount of dichloromethane, diethyl ether was added thereto, the produced solid was collected by filtration, and then washed with diethyl ether. A white solid of highly purified Compound 23 (1.47 g, yield 82%) was obtained.
1H NMR (500 MHz, CD3OD) δ: 139 (t, 3H, J=7.5 Hz), 1.48 (quint, 4H, J=7.5 Hz), 1.71 (quint., 4H, J=7.5 Hz), 1.75 (quint., 4H, J=7.5 Hz), 2.44 (t, 4H, J=7.5 Hz), 2.95 (t, 4H, J=7.5 Hz), 4.36 (q, 2H, J=7.5 Hz), 7.97 (d, 2H, J=1.8 Hz), 8.19 (s, 1H); LRMS (ESI): m/z 407 [M+H]+.
##STR00016##
N,N-Dimethylformamide (0.6 mL) was added to ammonium salt 10 (16.6 mg, 0.0346 mmol), and triethylamine (14 μL, 0.104 mmol) was then added to dissolve the salt. EZ-Link® NHS-Iminobiotin (4, 30 mg, 0.0691 mmol) was added, and the mixture was stirred at room temperature for 14 hours. The solvent was evaporated off under reduced pressure, the crude product was dissolved into methanol (0.5 mL), a 2-N aqueous sodium hydroxide solution (138 μL, 0.276 mmol) was added, and the mixture was stirred at room temperature for 22 hours. The produced white suspension was added with water (0.5 mL), the solid was washed with diethyl ether, collected by filtration, and further washed with an excessive amount of diethyl ether. The obtained crude product was purified by reversed-phase HPLC (YMC-Pack ODS-AM, gradient: 0-10-11-36-37-50 min; 0-0-2045-100-100% CH3CN in 0.1% TFA in MQ, ramp time=25 min (20-45%), tr=24.9 min). Title Compound 11 (26.0 mg, yield=71%, pale yellow amorphous matter) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.43 (quint., 8H, J=7.5 Hz), 1.56 (quint., 6H, J=7.5 Hz), 1.60-1.67 (m, 4H), 1.73 (quint., 6H, J=7.5 Hz), 2.19 (t, 4H, J=7.5 Hz), 2.40 (t, 4H, J=7.5 Hz), 2.81 (d, 2H, J=13.2 Hz), 2.99 (dd, 2, J=13.2, 4.6 Hz), 3.19 (td, 4H, J=6.9, 1.7 Hz), 3.27 (ddd, 2H, J=10.3, 5.8, 4.6 Hz), 4.52 (dd, 2H, J=8.0, 4.6 HZ), 4.71 (2H, J=8.0, 4.6 Hz), 7.95 (d, 2H, J=1.8 Hz), 8.17 (d, 1H, J=1.8 Hz);
LRMS (ESI): m/z 415 [M+2H]2+.
##STR00017##
To a N,N-dimethylformamide (0.3 mL) solution of bisiminobiotin 11 (17 mg, 0.0161 mmol) were added N,N′-diisopropylcarbodiimide (DIC, 5.0 μL, 0.0322 mmol) and 1-hydroxybenzotriazole monohydrate (HOBt.H2O, 4.9 mg, 0.0322 mmol). An N,N-dimethylformamide (0.15 mL) solution of amine 12 (8.0 mg, 0.0322 mmol) synthesized by a known method (Wilbur et al., Bioconjugate. Chem. (2010) 21, 1225) was added, and the mixture was stirred at 60° C. for 10 hours. The solvent was evaporated off under reduced pressure, water (1 mL) was added, the aqueous layer was washed with a mixed solvent (1:1) of ethyl acetate and diethyl ether, and the solvent was evaporated off under reduced pressure. The residue was added with a 2-N hydrochloric acid (1 mL), and then sonicated to dissolve the crude product. Water (1 mL) was then added, the aqueous layer was washed with diethyl ether and ethyl acetate, and the solvent was evaporated off under reduced pressure. The obtained crude product was purified by reversed-phase HPLC (YMC-Pack ODS-AM, gradient: 0-10-50-51-65 min; 10-10-30-100-100% CH3CN in 0.1% TFA in MQ, ramp time=40 min (10-30%), tr=43.5 min). Title Compound 13 (11.2 mg, yield=53%, pale yellow amorphous matter) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.39-1.48 (m, 8H), 1.56 (quint, 6H, J=7.5 Hz), 1.65 (sext., 4H, J=6.9 Hz), 1.69-1.80 (m, 6H), 2.20 (t, 4H, J=7.5 Hz), 2.40 (t, 4H, J=7.5 Hz), 2.82 (d, 2H, J=13.2 Hz), 2.99 (dd, 2H, J=13.2, 4.6 Hz), 3.10 (t, 2H, J=5.2 Hz), 3.18 (t, 4H, J=7.5 Hz), 3.29 (ddd, 2H, J=10.3, 5.8, 4.6 Hz), 3.58 (t, 2H, J=5.2 Hz), 3.69 (quint, 8H, J=5.2 Hz), 4.52 (dd, 2H, J=8.0, 4.6 Hz), 4.72 (2H, dd, J=8.0, 4.6 Hz), 7.77 (d, 2H, J=1.7 Hz), 7.90 (d, 1H, J=1.7 Hz); LRMS (ESI): m/z 480 [M+2H]2+.
##STR00018##
To a methanol (02 mL) solution of bisiminobiotin 13 (5 mg, 3.84 μmol) were added triethylamine (4.3 μL, 30.7 μmol) and fluorescein-5-isothiocyanate (FITC, 1.6 mg, 4.03 μmol). The mixture, with a reddish brown solid deposited therein, was stirred at room temperature for 10 hours. Methanol (1 mL) was added, the mixture was sonicated, the solid was collected by suction filtration, and then washed with methanol. The solid was dissolved into a methanol solution containing 10% of trifluoroacetic acid. The solvent was evaporated off under reduced pressure, and the obtained yellow crude product was purified by reversed-phase HPLC (YMC-Triart-C18, detected at 270 nm, gradient: 0-10-11-4142-55 min; 20-20-30-60-100-100% CH3CN in 0.1% TFA in MQ, ramp time=30 min (30-60%), tr=25.7 min). Title Compound 14 (4.8 mg, yield=79%, pale yellow amorphous matter) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.41 (quint., 8H, J=7.5 Hz), 1.54 (quint., 6H, J=7.5 Hz), 1.63 (sext., 4H, J=6.9 Hz), 1.66-1.78 (m, 6H), 2.18 (t, 4H, J=7.5 Hz), 2.38 (t, 4H, J=7.5 Hz), 2.80 (2H, d, J=13.2 Hz), 2.97 (dd, 2H, J=13.2, 4.6 Hz), 3.17 (t, 4H, J=6.9 Hz), 3.26 (ddd, 2H, J=10.3, 5.8, 4.6 Hz), 3.57 (t, 2H, J=5.2 Hz), 3.68-3.74 (m, 8H), 3.81 (brs, 2H), 4.50 (dd, 2H, J=8.0, 4.6 Hz), 4.70 (d, 2H, J=7.5, 4.6 Hz), 6.73 (d, 2H, J=8.0 Hz), 6.87 (s, 2H), 6.92 (d, 2H, J=8.0 Hz), 720 (d, 1H, J=8.1 Hz), 7.72 (s, 2H), 7.82 (d, 1H, J=8.1 Hz), 7.96 (s, 1H), 828 (s, 1H); LRMS (ESI): m/z 675 [M+2H]2+.
##STR00019##
N,N-Dimethylformamide (0.23 mL) and triethylamine (4.8 μL, 0.034 μmmol) were added to diamine 10 (5.5 mg, 0.011XX mmol), EZ-Link® NHS-Iminobiotin 4 (10 mg, 0.023 mmol) was then added, and the mixture was stirred at room temperature for 6 hours. The solvent was evaporated off under reduced pressure, the crude product was dissolved into methanol (0.5 mL), 25% aqueous ammonia (2 mL) was added, and the mixture was stirred at 35° C. for 12 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase HPLC (YMC-Pack ODS-AM, gradient: 0-10-11-36-37-50 min; 0-0-20-45-100-100% CH3CN in 0.1% TFA in MQ, ramp time=25 min (20-45%), tr=23.1 min). Title Compound 15 (5.9 mg, yield=49%) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.38-1.46 (m, 8H), 1.56 (quint, 6H, J=7.5 Hz), 1.64 (sext, 4H, J=6.9 Hz), 1.73 (quint, 6H, J=7.5 Hz), 2.19 (t, 4H, J=7.5 Hz), 2.40 (t, 4H, J=7.5 Hz), 2.81 (d, 2H, J=13.2 Hz), 2.99 (dd, 2H, J=13.2, 4.6 Hz), 3.19 (t, 4H, J=6.9 Hz), 3.29 (ddd, 2H, J=10.3, 5.8, 4.6 Hz), 4.52 (dd, 2H, J=8.0, 4.6 Hz), 4.72 (dd, 2H, J=8.0, 4.6 Hz), 7.75 (d, 2H, J=1.7 Hz), 8.03 (d, 2H, J=1.7 Hz);
LRMS (ESI): m/z 829 [M+H]+.
##STR00020##
To a N,N-dimethylformamide (5 mL) solution of 5-(4-iodobenzamido)isophthalic acid 16 (0.50 g, 1.21 mmol) synthesized by a known method (Wilbur et al., Bioconjugate. Chem. (1997) 8, 161), added were 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl, 0.556 g, 2.90 mmol) and 1-hydroxybenzotriazole monohydrate (HOBt.H2O, 0.444 g, 2.90 mmol), further added was an N,N-dimethylformamide (1 mL) solution of amine 12 (0.663 g, 2.67 mmol) synthesized by a known method (Wilbur et al., Bioconjugate. Chem. (2010) 21, 1225), and the mixture was stirred at room temperature for 18 hours. After the solvent was evaporated off under reduced pressure, ethyl acetate and 0.5-N hydrochloric acid were added, the product was extracted with ethyl acetate, and the organic layer was washed successively with 0.5-N hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution, and a saturated sodium chloride solution. After the organic layer was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (ethyl acetate→dichloromethane/methanol=10:1). Title Compound 17 (380 mg, yield=36%, highly viscous yellow oil) was thus obtained.
1H NMR (400 MHz, CD3OD) δ: 1.40 (s, 18H), 3.20 (t, 4H, J=5.4 Hz), 3.51 (t, 4H, J=5.4 Hz), 3.58-3.71 (m, 16H), 7.73 (dt, 2H, J=8.5, 1.8 Hz), 7.92 (dt, 2H, J=8.5, 1.8 Hz), 8.03 (t, 1H, J=1.4 Hz), 8.30 (d, 1H, J=1.4 Hz); LRMS (ESI): m/z 894 [M+Na]+.
##STR00021##
To a dichloromethane (1 mL) solution of dicarbamate compound 17 (0.350 g, 0.401 mmol) was added trifluoroacetic acid (2 mL), and the mixture was stirred at room temperature for one hour. The solvent was evaporated off under reduced pressure, and the residue was washed with diethyl ether. The product was dissolved in methanol (1 mL), applied to Amberlite® IRA-400 column (basic resin, 20 mm×200 mm), and eluted with methanol. After the solvent was evaporated off under reduced pressure, the residue was dried in vacuo. Title Compound 18 (0.258 g, yield 96%, yellow amorphous matter) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 2.74 (t, 4H, J=5.2 Hz), 3.49 (t, 4H, J=5.2 Hz), 3.59 (t, 4H, J=5.2 Hz), 3.60-3.63 (m, 4H), 3.64-3.69 (m, 8H), 7.69 (dt, 2H, J=8.6, 1.8 Hz), 7.85 (dt, 2H, J=8.6, 1.8 Hz), 7.99 (t, 1H, J=1.7 Hz), 8.27 (d, 2H, J=1.7 Hz); LRMS (ESI): m/z 672 [M+H]+.
##STR00022##
To an N,N-dimethylformamide (17 mL) solution of Boc-Asp(otbu)-OH 19a (0.50 g, 1.73 mmol) and N-hydroxysuccinimide (0.343 g, 2.08 mmol) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl, 0.399 g, 2.08 mmol), and the mixture was stirred at room temperature for 11 hours. After the solvent was evaporated off under reduced pressure, the mixture was added with ethyl acetate and 0.5-N hydrochloric acid, the product was extracted into ethyl acetate, the organic layer was washed successively with 0.5-N hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution, and a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, and the solvent was evaporated off under reduced pressure. Title Compound 19 (0.431 g, yield 63%, white solid) was thus obtained. The obtained product was used for the next reaction without further purification.
1H NMR (400 MHz, CD3OD) δ: 1.45 (s, 9H), 1.47 (s, 9H), 2.84 (s, 4H), 3.09 (dd, 1H, J=17.5, 6.4 Hz), 3.18 (dd, 1H, J=17.4, 5.8 Hz), 4.46 (t, 1H, J=5.8 Hz); LRMS (ESI): m/z 387 [M+H]+.
##STR00023##
To a mixed solution of dioxane (0.8 mL) and pyridine (0.1 mL) containing diamine 18 (35.9 mg, 0.0412 mmol), activated ester 19 (33.4 mg, 0.0865 mmol) was added. The mixture was stirred at room temperature for 14 hours, an additional portion of activated ester 19 (10 mg, 0.0259 mmol) was added, and the mixture was stirred at room temperature for 6 hours. After the solvent was evaporated off under reduced pressure, the residue was added with ethyl acetate and 0.5-N hydrochloric acid, the product was extracted into ethyl acetate, the organic layer was washed successively with 0.5-N hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution, and a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol=25:1→15:1). Title Compound 20 (47.9 mg, yield=90%, yellow amorphous matter) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.42 (s, 18H), 1.43 (s, 18H), 2.53-2.67 (m, 4H), 3.32 (t, 4H, J=5.2 Hz), 3.53 (td, 4H, J=5.2, 1.7 Hz), 3.60-3.64 (m, 8H), 3.65-3.70 (m, 8H), 4.32 (quint., 2H, J=5.8 Hz), 7.72 (dt, 2H, J=8.6, 1.7 Hz), 7.90 (dt, 2H, J=8.6, 1.7 Hz), 8.03 (t, 1H, J=1.7 Hz), 8.29 (d, 2H, J=1.7 Hz); LRMS (ESI): m/z 1236 [M+Na]+.
##STR00024##
Trifluoroacetic acid (2.0 mL) was added to compound 20 (41 mg, 0.0338 mmol) to dissolve it therein, and the mixture was stirred at room temperature for 30 minutes. The solvent was evaporated off under reduced pressure, and the residue was added with diethyl ether, so that white solid was deposited. The solid was collected by suction filtration, washed with diethyl ether, and dried in vacuo. Title Compound 21 (30.4 mg, yield=80%, white solid) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 2.64 (dd, 2H, J=17.2, 7.5 Hz), 2.81 (dd, 2H, J=17.2, 4.0 Hz), 3.35 (t, 4H, J=5.2 Hz), 3.55 (t, 4H, J=5.2 Hz), 3.60-3.64 (m, 8H), 3.67-3.73 (m, 8H), 4.14 (dd, 2H, J=7.5, 4.0 Hz), 7.74 (d, 2H, J=8.6 Hz), 7.92 (d, 2H, J=8.6 Hz), 8.05 (t, 1H, J=1.2 Hz), 8.29 (d, 2H, J=1.2 Hz);
LRMS (ESI): m/z 902 [M+H]+.
##STR00025##
Bisamino acid 21 (5 mg, 4.43 μmol) was dissolved into a mixed solvent of dioxane (0.2 mL) and water (0.1 mL), and a 1-N aqueous sodium hydroxide solution (18 μL, 177 μmol) was then added. The mixture was stirred at room temperature for 5 minutes, and then added with EZ-Link® NHS-Iminobiotin (4, 4.0 mg, 9.07 μmol). The mixture was stirred at room temperature for 19 hours, added with a 2-N aqueous sodium hydroxide solution (150 μL), and the mixture was further stirred at room temperature for 4 hours. The aqueous layer was washed with diethyl ether, and the solvent was evaporated off under reduced pressure. The obtained crude product was purified by reversed-phase HPLC (YMC-Pack ODS-AM, gradient 0-10-11-36-37-50 min; 0-0-24-49-100-100% CH3CN in 0.1% TFA in MQ, ramp time=25 min (24-49%), tr=27.2 min). Title Compound 22 (2.3 mg, yield=33%, white solid) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.40-1.51 (m, 4H), 1.52-1.81 (m, 8H), 2.25 (sext., 4H, J=7.2 Hz), 2.73 (d, 4H, J=6.3 Hz), 2.81 (d, 2H, J=13.4 Hz), 2.98 (dd, 2H, J=13.4, 4.5 Hz), 3.24-3.31 (m, 2H), 335 (t, 4H, J=5.4 Hz), 3.54 (t, 4H, J=5.4 Hz), 3.60-3.65 (m, 8H), 3.66-3.72 (m, 8H), 4.53 (dd, 2H, J=8.1, 4.5 Hz), 4.70-4.74 (m, 4H), 7.74 (d, 2H, J=8.5 Hz), 7.93 (d, 2H, J=8.5 Hz), 8.05 (s, 1H), 8.31 (d, 2H, J=1.4 Hz); LRMS (ESI): m/z 677 [M+2H]+.
##STR00026##
To an N,N-dimethylformamide (1.6 mL) solution of diamine 3 (21.8 mg, 0.0659 mmol), biotin N-hydroxysuccinimide ester (23, 45 mg, 0.132 mmol) was added, and the mixture was stirred at room temperature for 6 hours. The mixture was added with diethyl ether, and the deposited solid was collected by filtration. The solid was washed successively with 1-N hydrochloric acid, a saturated sodium carbonate solution, water, cold acetone, and diethyl ether, and then dried in vacuo. Title Compound 24 (46.2 mg, yield=90%, white solid) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.32-1.38 (m, 4H), 1.44 (quint., 4H, J=7.5 Hz), 1.52 (quint., 4H, J=7.5 Hz), 1.58-1.69 (m, 10H), 1.69-1.78 (m, 2H), 2.20 (q, 8H, J=7.5 Hz), 2.71 (d, 2H, J=13.2 Hz), 2.93 (dd, 2H, J=12.6, 4.6 Hz), 3.17 (t, 4H, J=6.9 Hz), 3.21 (ddd, 2H, J=10.3, 5.8, 4.6 Hz), 3.35 (t, 4H, J=5.8 Hz), 3.51 (t, 4H, J=5.8 Hz), 4.31 (dd, 2H, J=8.1, 4.6 Hz), 4.49 (dd, 2H, J=8.1, 4.6 Hz); LRMS (ESI): m/z 805 [M+Na]+.
List of Compounds Used in Example 2 and Thereafter:
##STR00027## ##STR00028##
Iminobiotin longtail may be synthesized as described below.
##STR00029##
To a mixed solution of dioxane (500 μL) and H2O (500 μL) containing 6-aminohexanoic acid (3 mg, 0.023 mmol), an aqueous sodium hydroxide solution was added to adjust pH to 9 or around. Compound 101 (10 mg, 0.023 mmol) (commercial product) was added, the mixture was stirred for 12 hours, added with ether, and the organic layer was removed. The aqueous layer was neutralized with hydrochloric acid, and then filtered. The residue was washed with acetone, and the solvent was evaporated off under reduced pressure. The obtained solid was dissolved into dioxane (500 μL) and H2O (500 μL), 29% aqueous ammonia was added, and the mixture was stirred for 3 hours. The solvent was evaporated off under reduced pressure, and the obtained crystal was washed with a dichloromethane-methanol mixed solvent. Four milligrams of iminobiotin longtail (yield 49%, white solid) was thus obtained.
MS (ESI) m/z 357 (M+H)+
General Method
Nuclear Magnetic Resonance (NMR) spectrum was measured using JEOL ECX500 (1H NMR: 500 MHz) or JEOL ECS400 (1H NMR: 400 MHz) spectrometer. Chemical shift was given in ppm, as a value away from an internal reference peak assignable to a residual solvent in a deuterated solvent (CDCl3: δ=7.26 ppm, CD3OD: δ=3.31 ppm, acetone-d6: δ=2.05 ppm, D2O: δ=4.79 ppm)). Low-resolution mass spectrum (ESI) was measured using Waters ZQ4000 spectrometer or Agilent 6120 Quadrupole LC/MS (ES) coupled with Agilent Technologies 1290 Infinity LC. Column chromatography was carried out using silica gel Merk 60 (230-400 mesh ASTM). Gel filtration chromatography was carried out using Sephadex LH-20 Lab Packs as a carrier. The reactions were monitored by thin layer chromatography (TLC), or low-resolution mass spectrometry (LRMS).
Reversed-phase high performance liquid chromatography (HPLC) was carried out using JASCO-HPLC system. Ultraviolet radiation of 210 nm or 254 nm was used for detection, and a gradient solvent system (acetonitrile/0.1% trifluoroacetic acid in MQ) was used as the mobile phase. Analysis was carried out using YMC-Triart-C18 column (150×4.6 mL) at a flow rate of 1 mL/min. Fractionation was carried out using YMC-Triart-C18 column (250×10 mL) at a flow rate of 3.5 mL/min.
EZ-Link (registered trademark) NHS-Iminobiotin was purchased from Thermo Fisher Scientific Inc. DOTA-NHS-ester was purchased from Macrocyclics, Inc. Other reagents were purchased from Aldrich, Tokyo Chemical Industry Co., Ltd. (TCI), Kanto Chemical Co., Inc. (Kanto), Wako Pure Chemical Industries, Ltd., and Watanabe Chemical Industries, Ltd. All reagents and solvents were used as sold, unless otherwise specifically noted.
##STR00030##
To a toluene solution (20 mL) of dimethyl 5-aminoisophthalate 25 (1.00 g, 4.78 mmol), triphosgene (1.48 g, 4.99 mmol) was added, and the mixture was stirred under reflux for 3 hours. The mixture was then added with pyridine, and stirred under reflux for one hour. The solvent was evaporated off under reduced pressure, the resultant crude product 26 was added with a mixed solvent of dichloromethane (25 mL) and triethylamine (728 μL, 5.24 mmol), further added with amine 27 (1.84 g, 6.52 mmol), and the mixture was stirred at room temperature for one hour. After the solvent was evaporated off under reduced pressure, the residue was added with 1-M hydrochloric acid, the product was extracted into ethyl acetate, the organic layer was washed three times with 1-N hydrochloric acid, and once with a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol=20:1→4:1). Title Compound 28 (1.06 g, yield 43%, yellowish white solid) was thus obtained.
1H NMR (400 MHz, CD3OD) δ: 3.27-335 (m, 2H), 3.39 (t, 21, J=5.5 Hz), 3.55 (t, 2H, J=5.5 Hz), 3.58 (t, 2H, J=5.5 Hz), 3.63 (s, 4H), 3.91 (s, 6H), 5.06 (s, 2H), 7.20-7.47 (m, 5H), 8.21 (t, 1H, J=1.4 Hz), 8.28 (d, 2H, J=1.4 Hz); LRMS (ESI): m/z 540 [M+Na]+.
##STR00031##
To a tetrahydrofuran (11.7 mL) solution of diester compound 28 (1.06 g, 2.05 mmol) was added a water (2.07 mL) solution of potassium hydroxide (1.15 g, 10.5 mmol), and the mixture was stirred at room temperature for 8 hours. Water was added until the deposited precipitate dissolved, and the solution was washed once with diethyl ether. The solution was added with 2-M hydrochloric acid, the product was extracted into ethyl acetate, and the organic layer was washed once with a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, and the solvent was evaporated off under reduced pressure. A crude product (white solid) containing title compound 29 was thus obtained. The obtained crude product was used for the next reaction without further purification.
1H NMR (500 MHz, CD3OD) δ: 3.18-3.34 (m, 2H), 3.39 (t, 2H, J=5.7 Hz), 3.56 (t, 2H, J=5.7 Hz), 3.58 (t, 2H, J=5.2 Hz), 3.63 (s, 4H), 5.06 (s, 2H), 7.23-739 (m, 5H), 8.25 (brs, 1H), 8.28 (brs, 2H); LRMS (ESI): m/z 512 [M+Na]+.
##STR00032##
To an N,N-dimethylformamide (11.1 mL) solution of dicarboxylic acid 29 (1.09 g, 2.23 mmol) were added N-hydroxysuccinimide (0.615 g, 5.34 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl, 1.03 g, 5.34 mmol), and the mixture was stirred, in an argon atmosphere, at room temperature for 24 hours. After the solvent was evaporated off under reduced pressure, the residue was added with 0.5-M hydrochloric acid, extracted into ethyl acetate, and the organic layer was washed three times with 0.5-M hydrochloric acid, once with an aqueous saturated sodium hydrogen carbonate solution, and once with a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, and the solvent was evaporated off under reduced pressure. Title Compound 30 (1.2 g, yield 79%, white solid) was thus obtained.
1H NMR (400 MHz, CD3OD) δ: 2.90 (s, 8H), 3.25-3.35 (m, 2H), 339 (t, 2H, J=5.5 Hz), 3.54 (t, 2H, J=5.5 Hz), 3.58 (t, 2H, J=5.5 Hz), 3.62 (s, 4H), 5.05 (s, 2H), 7.20-7.40 (m, 5H), 8.36 (brs, 1H), 8.52 (brs, 2H); LRMS (ESI): m/z 342 [M+2H]2+.
##STR00033##
To a mixed solution of N,N-dimethylformamide (18.1 mL) and triethylamine (1.48 mL, 10.6 mmol) containing disuccinimide compound 30 (1.21 g, 1.76 mmol) was added Na-Boc-L-lysine (31) (974 mg, 3.52 mmol), and the mixture was stirred at room temperature for 10 hours. After the solvent was evaporated off under reduced pressure, the residue was added with water and 1-M hydrochloric acid, extracted into ethyl acetate, and the organic layer was washed once with a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, the obtained crude product was dissolved into a small amount of dichloromethane, and the precipitate deposited from diethyl ether was collected by suction filtration. Title Compound 32 (1.68 g, yield quant., white solid) was thus obtained.
1H NMR (400 MHz, CD3OD) δ: 1.41 (s, 18H), 1.45-1.57 (m, 4H), 1.57-1.77 (m, 6H), 1.77-1.94 (m, 2H), 3.24-3.34 (m, 2H), 3.34-3.49 (m, 6H), 3.55 (t, 2H, J=5.4 Hz), 3.58 (t, 2H, J=5.0 Hz), 3.63 (s, 4H), 3.93-4.18 (m, 2H), 5.06 (s, 2H), 7.23-7.46 (m, 5H), 7.81 (brs, 1H), 7.93 (brs, 2H), 8.51 (brs, 1H).
##STR00034##
A methanol (530 μL) solution of dicarbamate compound 32 (100 mg, 106 μmol) was cooled on an ice bath, diazomethane (2.0 M solution in diethyl ether, 350 μL, 700 μmol) was added, and the mixture was stirred on an ice bath for 5 minutes. The mixture was added with acetic acid, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol=20:1→10:1). Title Compound 33 (91.8 mg, yield=89%, highly viscous yellow oil) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.39-1.43 (m, 22H), 1.55-1.73 (m, 6H), 1.75-1.87 (m, 2H), 3.27-3.33 (m, 2H), 3.39 (m, 6H), 3.54 (t, 2H, J=5.7 Hz), 3.57 (t, 2H, J=5.2 Hz), 3.62 (s, 4H), 3.69 (s, 6H), 4.10 (t, 2H, J=5.2 Hz), 5.06 (s, 2H), 6.86-7.05 (m, 1H), 7.24-7.35 (m, 5H), 7.81 (s, 1H), 7.93 (s, 2H), 8.46 (brs, 11).
##STR00035##
To a water (2 mL) solution of dicarbamate compound 33 (89.9 mg, 92.3 μmol), trifluoroacetic acid (2 mL) was added, and the mixture was stirred at room temperature for 1.5 hours. After the solvent was evaporated off under reduced pressure, the residue was dried in vacuo. A crude product (highly viscous yellow oil) containing title compound 34 was thus obtained. The obtained crude product was used for the next reaction without further purification.
1H NMR (400 MHz, CD3OD) δ: 1.38-1.60 (m, 4H), 1.60-1.73 (sext., 4H, J=7.3 Hz), 1.77-2.10 (m, 4H), 3.23-3.32 (m, 2H), 3.32-3.43 (m, 6H), 3.54 (t, 2H, J=5.5 Hz), 3.57 (t, 2H, J=5.5 Hz), 3.62 (s, 4H), 3.81 (s, 6H), 4.05 (t, 2H, J=6.4 Hz), 5.05 (s, 2H), 7.20-7.37 (m, 5H), 7.84 (brs, 1H), 7.96 (brs, 2H); LRMS (ESI): m/z 774 [M+H]+.
##STR00036##
To a mixed solution of N,N-dimethylformamide (200 μL) and triethylamine (14.4 μL, 10.3 μmol) containing diamine 34 (10.0 mg, 10.3 μmol) was added EZ-Link® NHS-Iminobiotin 4 (9.0 mg, 20.7 μmol), and the mixture was stirred at room temperature for 21 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by gel filtration chromatography (methanol). Title Compound 35 (5.6 mg, yield=39%, highly viscous yellow oil) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.32-153 (m, 8H), 1.53-1.69 (m, 10H), 1.69-1.79 (m, 4H), 1.83-1.93 (m, 2H), 2.25 (q, 4H, J=6.9 Hz), 2.88 (d, 2H, J=12.6 Hz), 3.01 (dd, 2H, J=52, 12.6 Hz), 3.27-3.33 (m, 4H), 3.34-3.45 (m, 6H), 3.55 (t, 2H, J=5.2 Hz), 3.57 (t, 2H, J=5.2 Hz), 3.63 (s, 4H), 3.71 (s, 6H), 4.40 (dd, 2H, J=4.6, 9.2 Hz), 4.49 (dd, 2H, J=4.6, 8.6 Hz), 4.75 (dd, 2H, J=4.6, 8.6 Hz), 5.06 (s, 2H), 7.21-7.38 (m, 5H), 7.81 (brs, 1H), 7.95 (brs, 2H); LRMS (ESI): m/z 613 [M+2H]2+.
##STR00037##
To an aqueous (50 μL) solution of bisiminobiotin 35 (5.8 mg, 4.1 μmol), trifluoroacetic acid (1 mL) was added, and the mixture was stirred at 50° C. for 2 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% TFA in MQ, ramp time=40 min (17.5-57.5%), tr=36.5 min). Title Compound 36 (2.5 mg, yield=45%, highly viscous yellow oil) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.39-1.82 (m, 22H), 1.82-1.94 (m, 2H), 2.20-2.30 (m, 4H), 2.83 (d, 2H, J=14.2 Hz), 2.99 (dd, 2H, J=4.9, 14.2 Hz), 3.11 (t, 2H, J=5.2 Hz), 3.25-3.36 (m, 4H), 3.36-3.46 (m, 6H), 3.61 (t, 2H, J=5.3 Hz), 3.69 (s, 4H), 3.71 (s, 6H), 4.41 (dd, 2H, J=5.2, 9.7 Hz), 4.52 (dd, 2H, J=4.6, 8.1 Hz), 4.72 (dd, 5H, J=4.6, 8.1 Hz), 7.81 (s, 1H), 7.96 (d, 2H, J=1.6 Hz); LRMS (ESI): m/z 546 [M+2H]2+.
##STR00038##
To a mixed solution of N,N-dimethylformamide (100 μL) and triethylamine (15.1 μL, 10.9 mol) containing bisiminobiotin 36 (10.0 mg, 7.24 μmol), DOTA-NHS-ester 37 (6.1 mg, 7.96 μmol) was added, and the mixture was stirred at room temperature for 20 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% TFA in MQ, ramp time=40 min (17.5-57.5%), tr=35.2 min). Title Compound 38 (2.0 mg, yield=16%, highly viscous yellow oil) was thus obtained.
LRMS (ESI): m/z 739 [M+2H]2+.
Nuclear magnetic resonance (NMR) spectrum was measured using JEOL ECX500 (1H NMR: 500 MHz), or JEOL ECS400 (1H NMR: 400 MHz) spectrometer. Chemical shift was given in ppm, as a value away from an internal reference peak assignable to a residual solvent in a deuterated solvent (CDCl3: δ=7.26 ppm, CD3OD: δ=3.31 ppm). Low-resolution mass spectrum (ESI) was measured using Waters ZQ4000 spectrometer or Agilent 6120 Quadrupole LC/MS (ESI) coupled with Agilent Technologies 1290 Infinity LC. Column chromatography was carried out using silica gel Merk 60 (230-400 mesh ASTM), reversed-phase column chromatography was carried out using Wakosil® 40C18 (30 to 50 μm 70% up), and gel filtration chromatography was carried out using Sephadex LH-20 Lab Packs as a carrier. The reactions were monitored by thin layer chromatography (TLC), or low-resolution mass spectrometry.
Reversed-phase high performance liquid chromatography (HPLC) was carried out using JASCO-HPLC system. Ultraviolet radiation of 210 nm or 254 nm was used for detection, and a gradient solvent system (acetonitrile/0.1% trifluoroacetic acid in MQ, or a 0.1% formic acid in MQ) was used as the mobile phase. Analyses were carried out using YMC-Triart-C18 column (150×4.6 mL) at a flow rate of 1 mL/min. Fractionation was carried out using YMC-Triart-C18 column (250×10 mL) at a flow rate 3.5 mL/min.
DOTA-NHS-ester was purchased from Macrocyclics, Inc. IRDye® 800CW NHS Ester was purchased from LI-COR, Inc. Other reagents were purchased from Aldrich, Tokyo Chemical Industry Co., Ltd. (TCI, Kanto Chemical Co., Inc. (Kanto), Wako Pure Chemical Industries, Ltd., and Watanabe Chemical Industries, Ltd. All reagents and solvents were used as sold, unless otherwise specifically noted.
##STR00039##
Trifluoroacetic acid was added to 2-iminobiotin 39 (88.0 mg, 0.36 mmol), the mixture was stirred, and an excessive portion of trifluoroacetic acid was evaporated off under reduced pressure. To an acetonitrile solution (3.4 mL) of the thus obtained white solid, added were pyridine (82.5 μL, 0.72 mmol) and disuccinimide 40 (175 mg, 1.08 mmol), and the mixture was stirred for 11 hours at 30° C. The solvent was evaporated off under reduced pressure, and the residue was dried in vacuo. A crude product (highly viscous yellow oil) containing title compound 41 was obtained. The thus obtained crude product was used for the next reaction, without further purification.
LRMS (ESI): m/z 341 [M+H]+.
##STR00040##
To a solution of diamine 34 (78.5 mg, 81.1 μmol) dissolved in a mixed solvent of N,N-dimethylformamide (5.0 mL) and triethylamine (339 μL, 2.43 mmol) was added ester 41 prepared from 2-iminobiotin 39 (88.0 mg, 0.36 mmol), the mixture was then stirred at room temperature for 21 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase silica gel column chromatography (water/methanol=2:1→1:2). Title Compound 35 (59.3 mg, yield=52%, highly viscous yellow oil) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.32-1.53 (m, 8H), 1.53-1.69 (m, 10H), 1.69-1.79 (m, 4H), 1.83-1.93 (m, 2H), 2.25 (q, 4H, J=6.9 Hz), 2.88 (d, 2H, J=12.6 Hz), 3.01 (dd, 2H, J=5.2, 12.6 Hz), 3.27-3.33 (m, 4H), 3.34-3.45 (m, 6H), 3.55 (t, 2H, J=5.2 Hz), 3.57 (t, 2H, J=5.2 Hz), 3.63 (s, 4H), 3.71 (s, 6H), 4.40 (dd, 2H, J=4.6, 9.2 Hz), 4.49 (dd, 2H, J=4.6, 8.6 Hz), 4.75 (dd, 2H, J=4.6, 8.6 Hz), 5.06 (s, 2H), 7.21-7.38 (m, 5H), 7.81 (brs, 1H), 7.87 (brs, 2H); LRMS (ESI): m/z 613 [M+2H]2+.
##STR00041##
To a water (400 μL) solution of bisiminobiotin 35 (59.3 mg, 41.8 μmol) was added trifluoroacetic acid (8.0 mL), and the mixture was stirred at 50° C. for 4 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase silica gel column chromatography (water/methanol=2:1→1:2). Title Compound 36 (37.1 mg, yield=64%, highly viscous yellow oil) was thus obtained.
1H NMR (500 MHz, CD3OD) δ 1.39-1.82 (m, 22H), 1.82-1.94 (m, 2H), 2.20-2.30 (m, 4H), 2.83 (d, 2H, J=14.2 Hz), 2.99 (dd, 2H, J=4.9, 14.2 Hz), 3.11 (t, 2H, J=5.2 Hz), 3.25-3.36 (m, 4H), 3.36-3.46 (m, 6H), 3.61 (t, 2H, J=5.3 Hz), 3.69 (s, 4H), 3.71 (s, 61H), 4.41 (dd, 2H, J=5.2, 9.7 Hz), 4.52 (dd, 2H, J=4.6, 8.1 Hz), 4.72 (dd, 5H, J=4.6, 8.1 Hz), 7.81 (s, 1H), 7.96 (d, 2H, J=1.6 Hz); LRMS (ESI): m/z 546 [M+2H]2+.
##STR00042##
To a solution of bisiminobiotin 36 (23.4 mg, 16.9 μmol) dissolved in a mixed solvent of methanol (234 μL) and triethylamine (35.4 μL, 253 μmol) was added DOTA-NHS-ester 37 (25.8 mg, 24.9 μmol), and the mixture was stirred at room temperature for 13 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% HCOOH MQ, ramp time=40 min (17.5-57.5%), tr=31.5 min). Title Compound 42 (3.55 mg, yield=13%, highly viscous yellow oil) was thus obtained.
LRMS (ESI): m/z 739 [M+2H]2+.
##STR00043##
To a solution of bisiminobiotin 36 (1.13 mg, 0.82 μmol) dissolved in a mixed solvent of N,N-dimethylformamide (200 μL) and triethylamine (2.17 μL, 15.6 μmol) was added IRDye® 800CW NHS Ester (43, 2.41 mg, 2.06 μmol), and the mixture was stirred at room temperature for 17 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% TFA in MQ, ramp time=40 min (17.5-57.5%), tr=40.9 min). Title Compound 44 (0.65 mg, yield=34%, highly viscous green oil) was thus obtained.
LRMS (ESI): m/z 1038 [M+2H]2+.
##STR00044##
To an N,N-dimethylfomamide (1.9 mL) solution of disuccinimide compound 30 (198 mg, 0.290 mmol), added was amine 45 (118 mg, 0.580 mmol, N,N-dimethylformamide (1 mL) solution) synthesized by a known method (Arano et al., Bioorg. Med Chem. (2012) 20, 978), and the mixture was stirred at room temperature for 6.5 hours. Amine 45 (59 mg, 0.290 mmol, N,N-dimethylformamide (0.5 mL) solution) was further added, and the mixture was stirred at room temperature for 13 hours. After the solvent was evaporated off under reduced pressure, ethyl acetate was added, and the organic layer was washed successively with a 1-M aqueous sodium hydroxide solution, 1-M hydrochloric acid, and a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (dichloromethane/hexane=1:30→1:20→1:10→1:5). Title Compound 46 (83.7 mg, yield=33%, white solid) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.39 (s, 18H), 3.23 (t, 2H, J=5.7 Hz), 3.29-3.35 (m, 1H), 3.40 (t, 2H, J=5.7 Hz), 3.49-3.60 (m, 13H), 3.60-3.65 (m, 8H), 5.06 (s, 2H), 7.25-7.36 (m, 5H), 7.83 (s, 1H), 7.96 (brs, 2H); LRMS (ESI): m/z 884 [M+Na]+.
##STR00045##
To a water (400 μL) solution of dicarbamate compound 47 (26.6 mg, 31 μmol), trifluoroacetic acid (200 μL) was added under cooling on ice, the mixture was stirred for 30 minutes, heated to room temperature, and further stirred for 1.5 hours. After the solvent was evaporated off under reduced pressure, the residue was dried in vacuo. A crude product (34.0 mg, colorless liquid) containing title compound 48 was thus obtained. The obtained crude product was used for the next reaction without further purification.
1H NMR (400 MHz, CD3OD) δ: 3.14 (t, 2H, J=5.0 Hz), 3.29-3.35 (m, 1H), 3.41 (t, 2H, J=5.0 Hz), 3.53-3.65 (m, 13H), 3.67-3.73 (m, 8H), 5.06 (s, 2H), 7.24-7.37 (m, 5H), 7.85 (t, 1H, J=1.4 Hz), 7.98 (d, 2H, J=1.4 Hz); LRMS (ESI): m/z 662 [M+H]+.
##STR00046##
In a test tube containing compound 41 prepared from 2-iminobiotin 39 (16.6 mg, 68 μmol) were added an N,N-dimethylformamide (420 μL) solution of diamine 48 (252 mg) and diisopropylethylamine (40.1 μL, 23 μmol), and the mixture was stirred at room temperature for 12 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase silica gel column chromatography (methanol/water=2:1, 0.3% TFA). Title Compound 49 (28.8 mg, colorless liquid) was thus obtained.
1H NMR (500 MHz, CD3OD) δ: 1.33-1.41 (m, 4H), 1.47-1.62 (m, 6H), 1.64-1.72 (m, 2H), 2.17 (q, 4H, J=6.4 Hz), 2.80 (d, 2H, J=13.2 Hz), 2.97 (dd, 2H, J=4.6, 13.2 Hz), 3.20-3.25 (m, 2H), 3.29-3.35 (m, 1H), 3.35-3.42 (m, 6H), 3.53-3.61 (m, 13H), 3.63-3.67 (m, 8H), 4.49 (dd, 2H, J=4.6, 8.1 Hz), 4.71 (dd, 2H, J=5.2, 8.1 Hz), 5.07 (s, 2H), 7.24-7.38 (m, 5H), 7.88 (brs, 1H), 7.99 (brs, 2H).
##STR00047##
A mixed solvent of trifluoroacetic acid (1 mL) and water (50 μL) was added to bisiminobiotin 49 (6.9 mg, 5.3 μmol), the mixture was heated to 50° C., and stirred for 1.5 hours. After the solvent was evaporated off under reduced pressure, the residue was dried in vacuo. A crude product (5.3 mg, colorless liquid) containing title compound 50 was thus obtained. The obtained crude product was used for the next reaction without further purification.
1H NMR (500 MHz, CD3OD) δ: 1.32-1.43 (m, 4H), 1.47-1.62 (m, 6H), 1.63-1.74 (m, 2H), 2.13-2.20 (m, 4H), 2.81 (d, 2H, J=13.2 Hz), 2.98 (dd, 2H, J=4.6, 13.2 Hz), 3.08-3.14 (m, 2H), 3.20-3.27 (m, 2H), 3.35-3.45 (m, 6H), 3.52-3.73 (m, 20H), 4.51 (dd, 2H, J=4.6, 8.1 Hz), 4.72 (dd, 2H, J=5.2, 8.1 Hz), 7.87 (brs, 1H), 8.00 (brs, 2H).
##STR00048##
To a mixed solution of methanol (100 μL) and triethylamine (10 μL, 72 μmol) containing bisiminobiotin 50 (2.4 mg, 1.9 μmol), DOTA-NHS-ester 37 (3.5 mg, 4.6 μmol) was added, and the mixture was stirred at room temperature for 21 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase HPLC (0.0-20.0-20.5-60.5-61.0-75.0 min; 5.0-5.0-17.5-57.5-100.0-100.0% CH3CN in 0.1% TFA in MQ, ramp time=40 min (17.5-57.5%), tr=32.6 min). Title Compound 51 (highly viscous yellow oil) was thus obtained.
LRMS (ESI): m/z 683 [M+2H]2+.
##STR00049##
To a mixed solution of methanol (100 μL) and triethylamine (9.5 μL, 68 μmol) containing bisiminobiotin 50 (4.3 mg, 3.4 μmol) was added 5(6)-carboxyfluorescein N-hydroxysuccinimide ester 51 (4.8 mg, 10 μmol), and the mixture was stirred at room temperature for 16 hours. The solvent was evaporated off under reduced pressure, the obtained crude product was purified by reversed-phase column chromatography (methanol/water=1:1-2:1, 0.5% TFA), and further purified through Sephadex 20LH (methanol, 1% TFA). Title Compound 52 (2.2 mg, yield=49%) was thus obtained.
LRMS (ESI): m/z 669 [M+2H]2+.
##STR00050##
To a dichloromethane (480 μL) solution containing SN38 Boc-protected compound 53 (20.0 mg, 41 μmol) synthesized by a known method (Bioconjugate Chem. (2008) 19, 849.) and Cbz-Ala-OH 54 (12.7 mg, 57 μmol), added under cooling on ice were 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl, 12.7 mg, 66 μmol) and dimethylaminopyridine (1.5 mg, 12 μmol), the mixture was gradually heated to room temperature, and stirred for 11.5 hours. The mixture was added with dichloromethane, and washed successively with an aqueous sodium carbonate solution, water, 0.1-M hydrochloric acid, and a saturated sodium chloride solution. The organic layer was dried over sodium sulfate, the solvent was evaporated off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol=30:1). Title Compound 55 (26.8 mg, yield=95%, pale yellow solid) was thus obtained.
1H NMR (500 MHz, cdcl3) δ: 0.94 (t, 3H, J=7.5 Hz), 1.38 (t, 3H, J=7.4 Hz), 1.53 (d, 3H, J=6.9 Hz), 1.61 (s, 9H), 2.05-2.32 (m, 2H), 3.07-3.20 (m, 2H), 4.50-4.60 (m, 1H), 5.12-5.30 (m, 5H), 5.39 (d, 1H, J=17.2 Hz), 5.68 (d, 1H, J=17.2 Hz), 7.02-7.20 (m, 2H), 7.26-7.38 (m, 3H), 7.38-7.46 (m, 1H), 7.63 (dd, 1H J=9.2, 2.3 Hz), 7.89 (brs, 1H), 8.18 (d, 1H, J=9.2 Hz); LRMS (ESI): m/z 720 [M+Na]+.
##STR00051##
To an ethyl acetate solution (320 μL) of compound 55 (11.3 mg, 16 μmol), Pd/C (1.7 mg) was added, the atmosphere in the reaction vessel was replaced with hydrogen, the mixture was stirred at room temperature for 16 hours, then at 40° C. for one hour, and then filtered through celite. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by thin layer chromatography (dichloromethane/methanol=30:1). Title Compound 56 (2.3 mg, yield=26%) was thus obtained.
1H NMR (500 MHz, cdcl3) δ: 0.99 (t, 3H, J=7.5 Hz), 1.29 (t, 3H, J=8.0 Hz), 1.45 (d, 3H, J=6.9 Hz), 1.61 (s, 9H), 2.14-2.22 (m, 1H), 2.26-2.36 (m, 1H), 3.15 (q, 2H, J=8.0 Hz), 3.75 (q, 1H, J=6.9 Hz), 5.25 (d, 2H, J=3.5 Hz), 5.42 (d, 1H, J=17.2 Hz), 5.69 (d, 1H, J=17.2 Hz), 7.67 (dd, 1H J=9.2, 2.3 Hz), 7.90 (d, 1H, J=2.3 Hz), 8.21 (d, 1H, J=9.2 Hz).
##STR00052##
To a dichloromethane (100 μL) solution of compound 56 (2.3 mg, 4.1 μmol) were added triphosgene (3.3 mg, 11 μmol) and pyridine (5.0 μL, 62 μmol) under cooling on ice, the mixture was heated to room temperature, and stirred for 2 hours. After the solvent was evaporated off under reduced pressure, the residue was dried in vacuo. A crude product (brown liquid) containing title compound 57 was thus obtained. The obtained crude product was used for the next reaction without further purification.
##STR00053##
To a methanol (200 μL) solution of the crude product containing bisiminobiotin 50 (3.4 mg, 2.7 μmol) and compound 57, triethylamine (10 μL, 72 μmol) was added, and the mixture was stirred at room temperature for 15 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase thin layer chromatography (methanol/water=3:1, 1% TFA). Title Compound 58 (1.5 mg, yield=30%) was thus obtained.
LRMS (ESI): m/z 785 [M+2H]2+.
##STR00054##
To a water (100 μL) solution of bisiminobiotin 58 (1.5 mg, 0.8 μmol), trifluoroacetic acid (100 L) was added, and the mixture was stirred at room temperature for 1.5 hours. The solvent was evaporated off under reduced pressure, and the obtained crude product was purified by reversed-phase thin layer chromatography (methanol/water=3:1, 1% TFA). Title Compound 59 (0.4 mg, yield=29%) was thus obtained.
LRMS (ESI): m/z 735 [M+2H]2+.
A nucleotide sequence of a gene encoding wild-type core streptavidin is represented by SEQ ID NO: 1 in the Sequence Listing. In this invention, mcSA314 (also referred to as LISA314WT or LISA314 in this specification), described in International Patent WO2010/09455 as a low-immunogenic (modified) streptavidin, was used. mcSA314 is a streptavidin mutant having all types of mutations listed below, in the amino acid sequence of the core streptavidin represented by SEQ ID NO: 2:
(1) mutation given by substitution of tyrosine at position 10 with serine;
(2) mutation given by substitution of tyrosine at position 71 with serine;
(3) mutation given by substitution of arginine at position 72 with lysine;
(4) mutation given by substitution of glutamic acid at position 89 with aspartic acid;
(5) mutation given by substitution of arginine at position 91 with substituted with lysine; and
(6) mutation given by substitution of glutamic acid at position 104 with asparagine.
Oligo DNA used for producing each mutant was designed according to a manual attached to primerSTAR Mutagenesis Basal Kit (Takara Bio Inc.), so as to have an overlapped part over 15 bases on the 5′ terminus. Using the primers below, and using pCold TF vector having LISA314 inserted therein as a template, a codon sequence was altered by substituting the nucleotide sequence according to the site-directed mutagenesis method, to thereby convert the amino acid sequence. The template plasmid was then cleaved using restriction enzyme DpnI, and E. coli was transformed.
Primers:
(SEQ ID NO: 5)
LISA314 V21 Fw:
TGGAGCgatCAGCTGGGCgatACCTTT
(SEQ ID NO: 6)
LISA314 V21 Rv:
CAGCTGatcGCTCCAGGTGCCGGTAAT
LISA314 V21 (also referred to as V21, hereinafter), which is a LISA314 mutant, has additional mutations of N23D and S27D in LISA314. N23D means a mutation given by substitution of asparagine (N) at the 11th amino acid residue in the amino acid sequence of the core streptavidin represented by SEQ ID NO: 2, with aspartic acid (D). S27D means a mutation given by substitution of serine (S) at the 15th amino acid residue in the amino acid sequence of the core streptavidin represented by SEQ ID NO: 2, with aspartic acid (D).
Summarizing the above, V21 is a streptavidin mutant having the mutations below in the amino acid sequence of the streptavidin represented by SEQ ID NO: 2:
(1) mutation given by substitution of tyrosine at position 10 with serine;
(2) mutation given by substitution of tyrosine at position 71 with serine;
(3) mutation given by substitution of arginine at position 72 with lysine;
(4) mutation given by substitution of glutamic acid at position 89 with aspartic acid;
(5) mutation given by substitution of arginine at position 91 with substituted with lysine;
(6) mutation given by substitution of glutamic acid at position 104 with asparagine;
(7) mutation given by substitution of asparagine at position 11 with aspartic acid; and
(8) mutation given by substitution of serine at position 15 with aspartic acid.
Oligo DNA used for producing further mutant of V21 was designed according to a manual attached to primerSTAR Mutagenesis Basal Kit (Takara Bio Inc.), so as to have an overlapped part over 15 bases on the 5′ terminus. Using the primers below, and using a vector having the above-described V21 inserted therein as a template, a codon sequence was altered by substituting the nucleotide sequence according to the site-directed mutagenesis method, to thereby convert the amino acid sequence. The template plasmid was then cleaved using restriction enzyme DpnI, and E. coli was transformed.
Primers:
(SEQ ID NO: 7)
S45N Fw:
TATGAAAACGCCGTGGGTAATGCGGAA
(SEQ ID NO: 8)
S45N Rv:
CACGGCGTTTTCATAGGTGCCGGTCAG
S45N means a mutation given by substitution of serine (S) at the 33rd amino acid residue in the amino acid sequence of the core streptavidin represented by SEQ ID NO: 2, with asparagine (N). In other words, mutant LISA314 V212 (also referred to as V212, hereinafter), which is obtained by introducing an additional amino acid mutation S45N in V21, is produced. The amino acid sequence of this mutant is represented by SEQ ID NO: 3 in the Sequence Listing.
[2] Expression and Purification of V212 Protein
V212 protein was expressed in E. coli (BL21 (DE3) strain), collected in the form of inclusion body, refolded by the dilution method, and then subjected to affinity purification and gel filtration purification, to obtain a tetramer fraction. More specifically, the purified inclusion body was dissolved overnight in a denaturing buffer (6 M guanidine hydrochloride, 50 mM Tris-HCl, 200 mM NaCl, 1 mM EDTA, pH8.0 at 4° C.). Since the solubilized liquid, when measured in terms of absorbance at 280 nm, showed a concentration value of 50 mg/mL, 100 μL (5 mg equivalent) of the solubilized liquid was added dropwise into 50 mL of a refolding buffer (50 mM Tris-HCl, 300 mM NaCl, 1 mM EDTA, 400 mM Arginine-HCl, pH8.0 at 4° C.) under stirring, and incubated allowed to stand still at 4° C. for two day as for. For stable refolding, the storage time was limited to two days. After the 2-day incubation storage, the product was subjected to affinity purification using Ni-NTA resin (cOmplete His-Tag Purification Resin; Roche), followed by purification by gel filtration (HiLoad 16/60 Superdex 200 pg, from GE Healthcare BioScience Corp.) to obtain a tetramer fraction.
[3] Method of Crystallizing V21 and V212
Complexes Conjugates of proteins and Compounds were purified as follows. The proteins refolded by the dilution method were concentrated by affinity purification through Ni-NTA resin, the solvent was replaced with PBS, Compound C was added at a molar ratio of 1:8, incubated for one hour, and then allowed to pass through a gel filtration column, to obtain a tetramer fraction. These purified products were concentrated to 10 mg/mL through an ultrafiltration column (Vivaspin 20).
Each product was crystallized by the sitting drop vapor diffusion method, at a crystallization temperature of 20° C. A drop prepared by mixing the protein and a reservoir solution (0.2 M sodium fluoride, 20% PEG 3350) at a ratio of 0.5 μL:0.5 μL was equilibrated with 60 μL of the reservoir solution. A 6% glycerol solution was used as an anti-freezing agent.
[4] Method of Crystallographic Analysis
Recovery intensity data was collected using SPring-8 BL44XU. The collected data was used to determine the phase of V212 crystal structure by using Phaser (molecular replacement program), based on previously-analyzed cocrystal data (
[5] Results of Crystallographic Analyses
Analysis of cocrystal structure formed between V212 and Compound C revealed an opened loop structure as shown in
In order to close the opened loop, it was supposedly necessary to suppress the hydrogen bonds formed between N45 and N49 (amino acids 33 and 37 in Sequence Listing 3). For this reason, asparagine (N) at position 37 in the amino acid sequence represented by SEQ ID NO: 3 was altered to alanine (A), glycine (G) or serine (S). These mutations are denoted as N49A, N49G and N49S, respectively. Method of expression was same as described previously. Using the primers below, mutant expressing vectors were constructed based on the site-directed mutagenesis.
Primer Set:
(SEQ ID NO: 9)
N49A Fw:
GTGGGTgcgGCGGAAAGCCGTTATGTT
(SEQ ID NO: 10)
N49A Rv:
TTCCGCcgcACCCACGGCattTTCATA
(SEQ ID NO: 11)
N49G Fw:
GTGGGTggtGCGGAAAGCCGTTATGTT
(SEQ ID NO: 12)
N49G Rv:
TTCCGCaccACCCACGGCattTTCATA
(SEQ ID NO: 13)
N49S Fw:
GTGGGTagcGCGGAAAGCCGTTATGTT
(SEQ ID NO: 14)
N49S Rv:
TTCCGCgctACCCACGGCattTTCATA
The mutant protein was expressed and purified in the same way as described above, by way of denaturation of the inclusion body, and refolding by the dilution method. The refolded and purified proteins, analyzed by SDS-PAGE, revealed that, as represented by
Microcal iTC200 (MicroCal, Northampton, Mass.) was used for the measurement.
Purified V2122 was dialyzed overnight against PBS at 4° C., and stock solutions of Compound C and biotin were prepared using the external dialysis solution. For the measurement, concentration of the stock solutions was adjusted to a ten-fold concentration of V2122 to be measured. Into a cell of a calorimeter, 25 μM of V2122 was placed, and each solution was added dropwise at a stirring speed of 1000 rpm at 25° C. Obtained data was analyzed using ORIGIN, and the titration curve was fitted based on the one-site binding isotherm.
Results are shown in
From the results of ITC, interaction between V2122 and Compound C was confirmed to be exothermic, suggesting a strong binding between them. Meanwhile, V2122 and biotin showed neither exothermic nor endothermic reaction, and were confirmed to be non-interactive.
(1) Preparation of Protein
A protein expression vector used herein for the immunogenicity testing was obtained by altering the above-described expression vector so as not to express T7-tag attached to the N terminus, using the primer set below, according to the site-directed mutagenesis method.
Primer Set:
(SEQ ID NO: 15)
T7tagRemove Fw:
tacatatgGCCGAAGCAGGTATTACC
(SEQ ID NO: 16)
T7tagRemove Rv:
CTTCGGCcatatgtatatctccttc
The target protein was expressed in E. coli (BL21(DE3) strain), collected in the form of inclusion body, refolded by the dilution method, and then subjected to affinity purification and gel filtration purification, to obtain a tetramer fraction. More specifically, the purified inclusion body was dissolved overnight in a denaturing buffer (6 M guanidine hydrochloride, 50 mM Tris-HCl, 200 mM NaCl, 1 mM EDTA, pH8.0 at 4° C.). After measuring the absorbance of the liquid at 280 nm, a portion of the solubilized liquid containing 5 mg of product was added dropwise into 50 mL of a refolding buffer (50 mM Tris-HCl, 300 mM NaCl, 1 mM EDTA, 400 mM Arginine-HCl, pH8.0 at 4° C.) under stirring, and allowed to stand still at 4° C. for two days for. For stable refolding, the storage time was limited to two days. After the 2-day storage, the product was subjected to affinity purification using Ni-NTA resin (cOmplete His-Tag Purification Resin; Roche), followed by purification by gel filtration (HiLoad 16/60 Superdex 200 pg, from GE Healthcare BioScience Corp.) using saline as a buffer, to obtain a tetramer fraction.
(2) Immunogenicity Testing
Immunogenicity testing was conducted using four crab-eating monkeys. One milligram of the purified protein was administered three times. Before administration, blood was collected for preparing a negative control serum, followed by three times of administration of 1 mg each of purified protein. More specifically, letting the first day of administration of Day 0, the second administration fell on Day 21, and the third administration fell on Day 42. For V2122, blood was collected on Days 7, 14, 28 and 35 to prepare serum samples, and for the other, blood was collected on Days 7, 14, 28, 35, 49 and 56 to prepare serum samples.
Antibody against V2122 in the serum samples was analyzed by surface plasmon resonance (SPR). More specifically, Biacore T200 (GE Healthcare BioScience Corp.) was used as a measuring instrument, which was operated in the mode using immunogenicity package. The sensor chip was CM5. As instructed by the manual, V2122 protein (10 μg/mL) was immobilized on the CM5 sensor chip using an amine coupling kit. Serum was diluted ten-fold with a running buffer (HBS-EP, GE Healthcare BioScience Corp.) for the interaction analysis. More specifically, the serum diluted ten-fold was loaded into the running buffer at a flow rate of 10 μL/min for 5 minutes. The obtained sensorgram was analyzed using an analytical software named Biacore T200 Evaluation Software.
Results are shown in
Interaction of V2122, which is a LISA314 modified protein purified as described above, with Compound C was investigated by surface plasmon resonance (SPR). More specifically, using Biacore T200 (GE Healthcare BioScience Corp.) as a measuring instrument, and Sensor Chip NTA (GE Healthcare BioScience Corp.) as a sensor chip, the protein was immobilized on the sensor chip by way of His-Tag having been fused to the core protein. The running buffer was prepared using HBS-P(+), as described in the manual. A two-fold dilution series was prepared in nine steps by diluting a 1600 nM solution using the running buffer. The affinity was measured in the kinetics mode, and acquired data was subjected to equilibrium analysis using Biacore T200 Evaluation Software to determine the affinity.
The dissociation constant (M) between V2122 and biotin was not detected, meanwhile the dissociation constant (M) between V2122 and bisiminobiotin (Compound 7) was found to be 3.15×10−9.
For the crystallographic analysis, used was a protein from which T7-Tag has been removed, same as that used in the immunogenicity testing. The protein was expressed in Escherichia coli BL21-codonplus RIL, which was cultured in 2×YT medium, and an inclusion body was collected. The collected inclusion body was dissolved in 6 M Gdn.HCl, pH1.5, refolded using are folding buffer (50 mM Tris-HCl, 300 mM NaCl, 1 mM EDTA, 400 mM Arginine-HCl, pH8.0 at 4° C.) according to the dilution method described above, and then allowed to stand still at 4° C. for two days for. For stable refolding, the storage time was limited to two days. After the 2-day storage, the product was subjected to affinity purification using Ni-NTA resin (cOmplete His-Tag Purification Resin; Roche), followed by purification by gel filtration (HiLoad 16/60 Superdex 200 pg, from GE Healthcare BioScience Corp.) using PBS as a buffer, to obtain a tetramer fraction.
The thus purified tetramer fraction was added with Compound C or Compound D at a molar ratio of 1:8, and the mixture was incubated for one hour. The mixture was then concentrated to 10 mg/mL through an ultrafiltration column (Vivaspin 20), while replacing the buffer with a 20 mM Tris-HCl, pH7.5, 200 mM NaCl.
(1) Co-Crystallization of V2122 and Compound C
The co-crystallization was carried out by the sitting drop vapor diffusion method, at a crystallization temperature of 20° C. A drop prepared by mixing the protein and a reservoir solution (0.2 M citrate tribasic dehydrate, 20/(w/V) PEG 3350) at a ratio of 0.1 μL:0.1 μL was equilibrated with 60 μL of the reservoir solution. A 25% glycerol solution was used as an anti-freezing agent.
(2) Co-Crystallization of V2122 and Compound D
The crystallization was carried out by the sitting drop vapor diffusion method, at a crystallization temperature of 20° C. A drop prepared by mixing the protein and a reservoir solution (0.2 M citrate tribasic dehydrate, 20% (w/v) PEG 3350) at a ratio of 0.5 μL:0.5 μL was equilibrated with 60 μL of the reservoir solution. Oil was used as an anti-freezing agent.
(3) Method of Crystal Analysis
Recovery intensity data was collected using SPring-8 BL44XU. The collected data was used to determine the phase, using Phaser (molecular replacement program), based cocrystal data of a model molecule formed between previously-analyzed cocrystal data of V21—and iminobiotin longtail complex as the search model. Refinement was carried out using REFMAC5.
Results of crystallographic analysis are shown in
Comparing with a V212 crystal bound with Compound C, the crystal structure of V2122 bound with Compound C was confirmed to be altered largely in its loop structure as a result of disappearance of interaction between amino acids NO. 45 and 49 (NOs. 33 and 37 in the amino acid sequence in SEQ ID NO: 4) as planned, to have a closed loop same as found in V21, proving an advantage of mutation N49G. Also a structural difference in the loop moiety was found when comparing the structures of (V2122)s bound with Compound C or Compound D shown in
A gene sequence of Rituximab-scFv-V2122 was obtained by artificial gene synthesis (Life Technologies Corp.). More specifically, amino acid sequences of light chain (VL) and heavy chain (VH) were extracted from the amino acid sequence of rituximab contained in the DrugBank database (www.drugbank.ca), and VL and VH were ligated using a linker (GGGS×4) in the order of VL-VH. For the artificial synthesis, LV-LH was further ligated with V2122 using a linker (SSGSGSA), and the product was optimized to the codon usage of E. coli. The nucleotide sequence and the amino acid sequence of Rituximab-scFv-V2122 are represented by SEQ ID NOs: 27 and 28. Positions of the individual sequences in the amino acid sequence represented by SEQ ID NO: 28 are listed below:
pelB signal sequence: amino acids NOs. 1-23
VL sequence: amino acid NOs. 24-130
Linker sequence 1: amino acid NOs. 131-148
VH sequence: amino acid NOs. 149-269
Linker sequence 2: amino acid NOs. 270-276
V2122 sequence: amino acid NOs. 277-405
6×His-Tag sequence: amino acid NOs. 406-411
The gene artificially synthesized as described above was introduced into pET21a(+), the protein was expressed in Escherichia coli BL21(DE3), and then collected in the form of inclusion body. The collected inclusion body was refolded as described in Non-Patent Literature (Yumura et al. 2013, Protein Science) and purified.
The thus refolded and purified Rituximab-scFv-V2122 was evaluated regarding binding potential with RAMOS (human Burkitt lymphoma) cell (JCRB Cell Bank), which is a CD20 positive cell. More specifically, Rituximab-scFv-V2122 was diluted with PBS into three concentrations (0.05, 0.5, 5 μg/mL). 1×106 cells were placed in a 1.5 mL tube, centrifuged at 400×g for 4 minutes, and the supernatant was discarded to collect the cells. The collected cells were added with 100 μL of the diluted Rituximab-scFv-V2122, mixed well, and then incubated on ice for 30 minutes. The content was centrifuged again, the supernatant was discarded, added with 1 mL of PBS to wash the cells, and the cells were then collected. To 100 μL of cell, added was 13 nM or 1.3 nM of FITC-Psyche, or, 0.5 μg/mL (3.3 nM) of Anti-His-Tag mAb-Alexa Flour 488 (Medical and Biological Laboratories Co., Ltd.), the content was mixed, and incubated on ice for 30 minutes. After the incubation, the content was centrifuged again, the supernatant was discarded, added with 1 mL of PBS to wash the cells, and the cells were then collected. The collected cells were suspended in 500 μL of PBS, and measured on a flow cytometer (guava easyCyte Single System; Merck Millipore).
Results are show in
Referring first to Assay Result A obtained by using Alexa Flour 488-labeled anti-His-Tag antibody (3.3 nM), shifts of fluorescence intensity were observed to be dependent on the concentration of Rituximab-scFv-V2122, proving that the thus prepared Rituximab-scFv-V2122 recognized CD20 on the RAMOS cell surface. Referring next to Assay Result B obtained by using FITC-labeled Compound B, shifts of fluorescence intensity were observed to be dependent on the concentration of Rituximab-scFv-V2122 similarly to the case with the labeled anti-His-Tag antibody. Since concentration-dependent shifts of fluorescence intensity were also confirmed at the individual concentrations of Compound (3 nM, 10 nM, 30 nM), this was the first to prove binding of the FITC-labeled Compound B with Rituximab-scFv-V2122.
First, using restriction enzyme sites NdeI and XhoI in the pET21a(+) vector, a vector having a wild-type core streptavidin sequence (Patent Literature 1, amino acid sequence in SEQ ID NO: 2) introduced therein was produced. Next, as a template for the vector, a mutant of Y43A or S45A (amino acids at positions 31 and 33 in the amino acid sequence in SEQ ID NO: 2 are substituted respectively) was produced by using the primer set listed below, by site directed mutagenesis. The target protein was expressed in Escherichia coli (BL21(DE3) strain), collected in the form of inclusion body, refolded by the dilution method, followed by affinity purification and gel filtration purification to obtain a tetramer forming fraction. More specifically, the purified inclusion body was dissolved overnight in a denaturing buffer (6 M guanidine hydrochloride, 50 mM Tris-HCl, 200 mM NaCl, 1 mM EDTA, pH8.0 at 4° C.). After measuring the absorbance of the liquid at 280 nm, a portion of the solubilized liquid containing 5 mg of product was added dropwise into 50 mL of a refolding buffer (50 mM Tris-HCl, 300 mM NaCl, 1 mM EDTA, 400 mM Arginine-HCl, pH8.0 at 4° C.) under stirring, and allowed to stand still at 4° C. for two days for. For stable refolding, the storage time was limited to two days. After the 2-day storage, the product was subjected to affinity purification using Ni-NTA resin (cOmplete His-Tag Purification Resin; Roche), followed by purification by gel filtration (HiLoad 16/60 Superdex 200 pg, from GE Healthcare BioScience Corp.) using PBS as a buffer, to obtain the tetramer fraction.
Using the thus purified two wild-type core streptavidin mutants (csa-Y43A, csa-S45A), purified LISA314 and V2122 protein, interaction with biotin (Sigma-Aldrich) was investigated by surface plasmon resonance (SPR). More specifically, using Biacore T200 (GE Healthcare BioScience Corp.) as a measuring instrument, and Sensor Chip NTA (GE Healthcare BioScience Corp.) as a sensor chip, the protein was immobilized on the sensor chip by way of His-Tag having been fused to the core protein. The running buffer was prepared using HBS-P(+), as described in the manual. A dilution series of Compound was prepared by using the running buffer in seven steps of 1.8 nM, 9 nM, 18 nM, 90 nM, 180 nM, 900 nM and 1800 nM, to obtain data.
Primer Set:
(SEQ ID NO: 17)
Y43A Fw:
GGCACCGCCGAAAGCGCCGTGGGTAAT
(SEQ ID NO: 18)
Y43A Rv:
GCTTTCGGCGGTGCCGGTCAGCGCACC
(SEQ ID NO: 19)
S45A Fw:
TATGAAGCCGCCGTGGGTAATGCGGAA
(SEQ ID NO: 20)
S45A Rv:
CACGGCGGCTTCATAGGTGCCGGTCAG
Results are shown in
Judging from the sensorgram, both of wild-type streptavidin mutants cSA-Y43A and cSA-S45A showed interaction in a biotin concentration-dependent manner, proving a strong specific binding with biotin, equivalent to that shown by LISA314 which can dissociate from biotin only extremely slowly. Meanwhile, V2122 did not show biotin concentration-dependent interaction, proving absence of specific binding. As a consequence, wild-type streptavidin mutants cSA-Y43A and cSA-S45A, and LISA314 were confirmed to be proteins totally different from V2122 in terms of interaction with biotin.
Using the purified two wild-type core streptavidin mutants (cSA-Y43A, cSA-S45A) described above, and purified V2122 protein, interaction with Compound C was investigated by surface plasmon resonance (SPR). More specifically, using Biacore T200 (GE Healthcare BioScience Corp.) as a measuring instrument, and Sensor Chip NTA (GE Healthcare BioScience Corp.) as a sensor chip, the protein was immobilized on the sensor chip by way of His-Tag having been fused to the core protein. The running buffer was prepared using HBS-P(+), as described in the manual. A dilution series of Compound was prepared by using the running buffer in seven steps of 1.8 nM, 9 nM, 18 nM, 90 nM, 180 nM, 900 nM and 1800 nM, to obtain data.
Results are shown in
From the measurement, wild-type streptavidin mutant cSA-Y43A showed a concentration-dependent interaction with Compound C but with a fast dissociation, meanwhile wild-type streptavidin mutant cSA-S45A showed only a very weak, concentration-dependent interaction with Compound C. In contrast, V2122 and Bis-iminobiotin showed a concentration-dependent interaction, characterized by a specific binding showing only an extremely slow dissociation. As a consequence, wild-type streptavidin mutants cSA-Y43A and cSA-S45A were confined to be proteins totally different from V2122 in terms of interaction with Compound C. Compound C and V2122 were confirmed to show a highly specific strong binding.
(1) Culture for Expression, and Purification of Anti-Epiregulin scFv Antibody
Escherichia coli was transformed with a plasmid encoding anti-epiregulin scFv. A colony of Escherichia coli was precultured in an LB liquid medium, the main culture was allowed to proceed in a 2×YT medium, and IPTG was added to induce expression of anti-epiregulin scFv. The collected bacterial cells were crushed in a Tris buffer, centrifuged, and the supernatant was collected. The supernatant was then purified successively through a Ni column, anion exchange column, and gel filtration column. Results of SDS-PAGE after the gel filtration are shown in
The antibody was crystallized at 20° C. by the sitting drop vapor diffusion method. A good crystal was obtained by preparing a drop by mixing the purified protein solution (15 mg/mL anti-epiregulin scFv), 20 mM Tris-HCl (ph 7.5), 300 mM NaCl) with a reservoir solution (2% Tacsimate (ph 7.0), 5% 2-propanol, 0.1 M imidazole (ph 7.0), 11% PEG 3350).
The obtained crystal was analyzed by X-ray diffractometry using SPring-8 BL44XU beam line to obtain diffraction data with a 2.4-A resolution. The data was processed using HKL2000 program, the phase was determined using Phaser based on the molecular replacement method, and the structure was further refined using Refmac5.
(2) Preparation, Crystallization and Structural Analysis of Conjugate of Anti-Epiregulin scFv and Epiregulin
Five milligrams each of anti-epiregulin scFv and epiregulin (extracellular domain) were mixed, and the mixture was incubated at 25° C. for one hour. The mixture was purified through a gel filtration column, to collect a conjugate fraction.
The conjugate was crystallized by the hanging drop vapor diffusion method at 20° C. A good crystal was obtained by preparing a drop by mixing a conjugate sample (15 mg/mL scFv-epiregulin complex, 20 mM Tris-HCl (ph 7.5), 300 mM NaCl) with a reservoir solution (0.1 M magnesium chloride, 0.1 M sodium acetate (pH 5.1), 10% PEG 6,000).
The obtained crystal was analyzed by X-ray diffractometry using SPring-8 BL32XU beam line to obtain diffraction data with a 1.8-Å resolution. The data was processed using HKL2000 program, the phase was determined using Phaser based on the molecular replacement method, and the structure was further refined using Refmac5.
(3) Recognition Mechanism of Epiregulin by Anti-Epiregulin scFv Antibody
Crystal structures of anti-epiregulin scFv in itself, and in the form of conjugate with epiregulin revealed the followings. There were three major sites where anti-epiregulin scFv and epiregulin can interact, which were roughly classified into interaction of the N-terminus region of epiregulin with CDR1 and CDR3 in the light chain of anti-epiregulin scFv (Interaction 1); interaction of the C-terminus region of epiregulin with CDR2 in the heavy chain of anti-epiregulin scFv (Interaction 2); and interaction of the β-sheet region of epiregulin with CDR3 in the heavy chain of anti-epiregulin scFv (Interaction 3). In interactions 1 and 2, the loop structure of epiregulin changed, but without distinct change in the structure of CDR in anti-epiregulin HM (scFv). In contrast, in the region of Interaction 3, the structure of epiregulin did not change, but with a structural change in CDR3 in the heavy chain of anti-epiregulin scFv, characterized by cis-trans isomerization of P103 residue, where antigen was found to be recognized by induced fit (
(1) Production of Anti-Epiregulin scFv-V2122 Expression Vector
It is widely known that a fusion protein of single chain variable region antibody and streptavidin (scFv-SA), when expressed in Escherichia coli, often forms an aggregate or inclusion body, and is difficult to be recovered in a solubilized form. For this reason, a standard procedure for obtaining scFv-SA protein is such as denaturing the inclusion body and refolding the protein. Production of protein by refolding is, however, time-consuming and labor-consuming. A method employed in this invention is such as allowing both of skp, which is a protein with chaperone function, and anti-epiregulin scFv-V2122 to be expressed in Escherichia coli, so that the protein becomes collectable in a soluble fraction.
More specifically, the gene sequence of chaperone skp (SEQ ID NO: 23) was designed to be suited to a codon used by Escherichia coli, based on the protein sequence (SEQ ID NO: 24). Meanwhile, the gene sequence of a fusion protein (anti-epiregulin scFv-V2122) formed by single chain variable region antibody of anti-epiregulin antibody (anti-epiregulin scFv) and V2122 was designed in such a way that the variable regions of anti-epiregulin antibody were ligated in the direction from VH to VL using a linker (GGGGS)×4 (SEQ ID NO: 35), and VL and V2122 were ligated with a linker (GGGGSGGGG) (SEQ ID NO: 36), and then suited to a codon used by Escherichia coli, in the same way as skp. These two gene sequences were artificially synthesized by Artificial Gene Synthesizing Service (Life Technologies Corp.). For the variable regions VH and VL, reference was made on Lee Y H, et al., Biochem. Biophys. Res. Commun., 2013 Nov. 29; 441(4):1011-7. doi: 10.1016/j.bbrc2013.11.014. Epub 2013 Nov. 12. PubMed PMID:24239549.
The nucleotide sequence and the amino acid sequence of the single chain variable region antibody of anti-epiregulin antibody (anti-epiregulin scFv) are represented by SEQ ID NOs: 21 and 22.
Positions of the individual sequences in the amino acid sequence represented by SEQ ID NO: 22 are listed below:
pelB signal sequence: amino acid NOs. 1-22
VH sequence: amino acid NOs. 23-140
Linker sequence 1: amino acid NOs. 141-164
VL sequence: amino acid NOs. 165-273
6×His-Tag sequence: amino acid NOs. 274-279
The nucleotide sequence and the amino acid sequence of the fusion protein formed by anti-epiregulin scFv and V2122 (anti-epiregulin scFv-V2122) are represented by SEQ ID NOs: 29 and 30.
Positions of the individual sequences in the amino acid sequence represented by SEQ ID NO: 30 are listed below:
pelB signal sequence: amino acid NOs. 1-22
VH sequence: amino acid NOs. 23-140
Linker sequence 1: amino acid NO. 141-164
VL sequence: amino acid NOs. 165-272
Linker sequence 2: amino acid NOs. 273-282
V2122 sequence: amino acid NOs. 283-409
6×His-Tag sequence: amino acid NOs. 410-415
Next, of these two artificially synthesized genes, the gene sequence of skp was introduced into multicloning site 1 (MCS1) of pETDuet-1 vector (from Novagen), and the gene sequence of anti-epiregulin scFv-V2122 was introduced into MCS2. More specifically, first, the vector chain was straightened using restriction enzyme NcoI, the gene sequence of skp was amplified by PCR using primers (MCS1_skp_Fw: AGGAGATATACCATGATGAAAAAATGGCTGCTGGC (SEQ ID NO: 37) and MCS1_skp_Rv: CGCCGAGCTCGAATITTATITCACTTGTITCAGAACG (SEQ ID NO: 38)), designed according to the manual of In-Fusion HD Cloning Kit (Clontech Laboratories, Inc.), purified from a cut gel, subjected to cloning using In-Fusion HD Cloning Kit based on ligation with the straightened vector, the cloned plasmid was then examined by sequence analysis, to select a target clone. Next, the plasmid vector having skp gene inserted therein was straightened using restriction NdeI, the gene sequence of anti-epiregulin scFv-V2122 was amplified in the same way as described above by PCR using primers (MCS2_scFvV2122_Fw; AAGGAGATATACATAATGAAATACCTATTGCCTACGOCAG (SEQ ID NO: 39) and MCS2 scFvV2122_Rv; TTGAGATCTGCCATATCAGTGGTGGTGGTGGTGGTGGCTG (SEQ ID NO: 40)), designed according to the manual of In-Fusion HD Cloning Kit (Clontech Laboratories, Inc.), purified from a cut gel, subjected to cloning using In-Fusion HD Cloning Kit based on ligation with the straightened vector, the cloned plasmid was then examined by sequence analysis, to select a target clone. In this way, a vector (pETDuet-epiregulin-scFvV2122_skp) capable of concurrently expressing skp protein and anti-epiregulin scFv-V2122 protein was completed.
(2) Expression of Anti-Epiregulin scFv-V2122 Protein
BL21(DE3) (Nippon Gene Co., Ltd.) was transformed with pETDuet-epiregulin-scFvV2122 skp, and precultured overnight in 2×YT medium (Sigma-Aldrich) at 37° C. The medium used for the preculture was added to a new medium in a 100-fold dilution, and the culture was continued at 37° C. until OD (600 nm) becomes 0.5 to 2.0. Next, a solution containing 1 mM IPTG and 1% Triton X-100 (final concentration), was added, and the content was cultured at 16° C. for 4 hours, the supernatant was collected, and stored at 4° C.
(3) Purification of Anti-Epiregulin scFv-V2122 Protein
Anti-epiregulin scFv-V2122 protein was partially purified based on the batch process, using 6×His-Tag having been attached to the C-terminus. More specifically, cOmplete His-Tag Purification Resin equilibrated with buffer A (50 mM Tris-HCl, 0.2 M NaCl, 1 mM EDTA, 5 mM imidazole, pH8.0) was added to the supernatant of culture having been stored at 4° C., and the mixture was stirred for 2 hours up to overnight at 4° C., so as to allow the resin to bind the protein. Next, the resin was collected in a column, and washed with 20 column volumes of buffer A. The column was then eluted with buffer B (50 mM Tris-HCl, 0.2 M NaCl, 1 mM EDTA, 400 mM imidazole, pH8.0), to collect a crude product of anti-epiregulin scFv-V2122.
Next, the protein was purified using a hydroxyapatite column (Bio-Scale CHT2-I) (Bio-Rad Laboratories, Inc.). More specifically, the crude product of anti-epiregulin scFv-V2122 was concentrated through Vivaspin Turbo 15 column (molecular weight cutoff: 30,000), and then using PD-10 column, the buffer of the crude product was replaced with a starling buffer (5 mM Na2PO4, pH7.0). The hydroxyapatite column was fully equilibrated using the starting buffer, and the crude product whose buffer had been replaced was applied to the column. After washing with 20 column volumes, the column was eluted with 15 column volumes of elution buffer (400 mM Na2PO4, pH7.0) with a gradient from 0% to 60%, to prepare a target purified product (
(4) Expression and Purification of Epiregulin IgG
Epiregulin IgG was expressed and purified making reference to Non-Patent Literature written by Lee et al. More specifically, gene sequences were artificially synthesized by ligating VL with a human light chain constant region, and by ligating VH with a human heavy chain constant region as described in the literature. They were denoted as light chain and heavy chain, respectively, of epiregulin IgG The nucleotide sequence and the amino acid sequence of the heavy chain of epiregulin IgG are represented by SEQ ID NOs: 31 and 32; and the nucleotide sequence and the amino acid sequence of the light chain of epiregulin IgG are represented by SEQ ID NOs: 33 and 34.
Next, the light chain and the heavy chain were introduced into pcDNA3.4 vector using pcDNA3.4 TOPO TA Cloning Kit (Life Technologies Corp.), to prepare expression vectors. The protein was expressed by introducing the vectors for the light chain and heavy chain in a ratio of 2:1, into Expi293F cell (Life Technologies Corp.) using ExpiFectamine 293 Transfection Kit. The cells were cultured following the usage and dosage instructions given in the manual of Expi293 Expression System Kit, at a CO2 concentration of 8% and number of rotation for shaking of 125 rpm, in a 1 L Erlenmeyer flast (Corning Inc.), on a thermostat shaker for mammalian cell C02-BR-43FL (Titec Corp.). After 5-day culture, the cells were removed by centrifugation, and the supernatant was collected and stored at 4° C. Next, epiregulin IgG was purified from the culture supernatant stored at 4° C., using Bio-Scale MiniUNOspher SUPrA affinity cartridge (Bio-Rad Laboratories, Inc.) following the usage and dosage instructions given in the manual.
Expression and Purification of Pro-EPR-mFc Protein (Pro-EPR-mFc), obtained by fusing the extracellular domain of epiregulin with the Fc region in the heavy chain of murine IgG1 antibody, was expressed and purified. The nucleotide sequence and the amino acid sequence of Pro-PR-mFc are represented by SEQ ID NOs: 25 and 26. More specifically, a gene produced by fusing the extracellular domain of epiregulin with the Fc region in the heavy chain of murine IgG1 antibody was introduced into pcDNA3.4 vector, and the protein was expressed and purified in the same way as described above in “Expression and Purification of Epiregulin IgG”.
(5) FITC Labeling of Purified Product, and Test of Labeled Product
An FITC-labeled product of the thus purified anti-epiregulin scFv-V2122 (anti-epiregulin scFv-V2122-FITC) was produced using Fluorescein Labeling Kit-NH (Dojindo Laboratories) following the usage and dosage instructions of the kit. Also epiregulin IgG and anti-epiregulin scFv protein were labeled in the same way.
Next, in order to confirm whether the labeling reduced the binding potential or not, the antigen binding potential of anti-epiregulin scFv-V2122-FITC was confirmed by SPR (Biacore T200). More specifically, protein (Pro-EPR-mFc) obtained by fusing the extracellular domain of epiregulin which functions as a ligand with murine Fe region is captured on the sensor chip CM5 having anti-Murine IgG antibody immobilized thereon, and then eluted for kinetics assay with an analyte composed of a two-fold dilution series prepared by diluting a 20 nM anti-epiregulin scFv-V2122-FITC solution into nine steps (
(6) Cell Staining Using Anti-Epiregulin scFv-V2122-FITC, and Analysis of Internalization
Human colorectal cancer-derived DLD1 cells, used for cell staining, were cultured in a complete medium RPNI1640 (containing 10% FBS), and seeded in uClear 96-well plate (Greiner) in a density of 1×104 cells/well, two days before the assay. In the cell staining, first the medium was replaced with a complete medium added with Hoechst 33342 so as to adjust the concentration to 1 μM, and 15 minutes after, each of anti-epiregulin scFv-V2122-FITC, epiregulin IgG-FITC and anti-epiregulin scFv-FITC was added to the individual wells so as to adjust the concentration to 25 nM, 50 nM and 100 nM.
Binding of antibody to the cell surface, and internalization were analyzed using IN Cell Analyzer 6000 (GE Healthcare BioScience Corp.), and recorded by time lapse imaging at 5 minute intervals.
From the study, staining of the surface of the cell membrane was observed for all of anti-epiregulin scFv-V2122-FITC, epiregulin IgG-FITC and anti-epiregulin scFv-FTC. A distinct internalization was observed particularly for anti-epiregulin scFv-V2122-FITC, which began to be observed approximately 10 minutes after the addition of antibody. Sixty-five minutes after, the almost entire part of fluorescence was found to migrate into the cytoplasm (
(7) FACS Analysis Using Anti-Epiregulin scFv-V2122-FITC
Cell surface binding potential was determined by FACS, using labeled antibodies that are anti-epiregulin scFv-V2122-FITC, epiregulin IgG-FITC and anti-epiregulin scFv-FITC. More specifically, dilute solutions of the labeled antibodies having concentrations of 0 nM, 0.5 nM, 5 nM and 50 nM were allowed to react on ice for 30 minutes with DLD1 cells (1×106 cells/mL, 500 mL) having epiregulin expressed therein, and then fluorescence was measured using flow cytometer guava easyCyte 5. The measurement followed the usage and dosage instructions given in the manual of the instrument.
In this study, among the labeled antibodies, anti-epiregulin scFv-V2122-FITC and epiregulin IgG-FITC showed equivalent levels of binding potential, whereas anti-epiregulin scFv-FITC showed a level of binding potential lower than those shown by the former two (
(1) Construction of Expression Vector
Rituximab single chain antibody (single chain variable fragment; scFv) was designed so that the light chain variable region VL and the heavy chain variable region VH were ligated in the order of VL and VH using a linker (GGGGS)×4. VL was attached with PelB sequence as a secretion signal, to produce a sequence of PelB-VL-(GGGGS)4—VH. scFv was ligated with V2122 using a linker (GGGGSGGGG) (referred to as Rituximab-scFv-V2122, hereinafter) (amino acid sequence: SEQ ID NO: 42). A gene sequence for expressing protein was synthesized by Artificial Gene Synthesizing Service (Life Technologies Corp.) (gene sequence: SEQ ID NO: 41). An expression vector was produced by incorporating Rituximab-scFv-V2122 to multicloning site 2 (MCS2) of pETDuet-1, in the same way as described in “(1) Production of Anti-Epiregulin scFv-V2122 Expression Vector” in Example 10.
The amino acid sequence and the nucleotide sequence of Rituximab-scFv-V2122 are shown below.
Gene Sequence of Rituximab-scFv-V2122
(SEQ ID NO: 41)
ATGAAATATCTGCTGCCGACCGCAGCAGCGGGTCTGCTGCTGCTGGCAGC
ACAGCCTGCAATGGCACAGATTGTTCTGAGCCAGAGTCCGGCAATTCTGA
GCGCATCACCGGGTGAAAAAGTTACCATGACCTGTCGTGCAAGCAGCAGC
GTTAGCTATATTCATTGGTTTCAGCAGAAACCGGGTAGCAGCCCGAAACC
GTGGATTTATGCAACCAGCAATCTGGCAAGCGGTGTTCCGGTTCGTTTTA
GCGGTAGCGGTAGTGGCACCAGCTATAGCCTGACCATTAGCCGTGTTGAA
GCAGAAGATGCAGCAACCTATTATTGTCAGCAGTGGACCAGTAATCCGCC
TACCTTTGGTGGTGGCACCAAACTGGAAATTAAAGGAGGTGGTGGTTCAG
GAGGTGGTGGTAGCGGTGGCGGTGGTAGCGGAGGTGGTGGTAGCCAGGTT
CAGCTGCAGCAGCCTGGTGCAGAACTGGTTAAACCGGGTGCAAGCGTTAA
AATGAGCTGTAAAGCAAGCGGTTATACCTTTACCAGCTACAATATGCATT
GGGTTAAACAGACACCGGGTCGTGGTCTGGAATGGATTGGTGCAATTTAT
CCGGGTAATGGTGATACGAGCTATAACCAGAAATTCAAAGGCAAAGCAAC
CCTGACCGCAGATAAAAGCAGCAGTACCGCCTATATGCAGCTGAGCAGTC
TGACCAGCGAAGATAGCGCAGTTTATTACTGTGCACGTAGCACCTATTAC
GGTGGTGATTGGTATTTTAACGTTTGGGGTGCAGGCACCACCGTTACCGT
TAGCGCAGGCGGAGGTGGAAGCGGTGGAGGTGGAGCAGAAGCAGGTATTA
CCGGCACCTGGTCAGATCAGCTGGGTGATACCTTTATTGTTACCGCAGGC
GCAGATGGTGCACTGACCGGTACATATGAAAATGCAGTTGGTAATGCAGA
AAGCCGTTATGTTCTGACCGGTCGTTATGATAGCGCACCGGCAACCGATG
GTAGCGGCACCGCACTGGGTTGGACCGTTGCATGGAAAAATAACAGCAAA
AATGCACATAGCGCAACCACATGGTCAGGTCAGTATGTTGGTGGTGCAGA
TGCCAAAATTAACACCCAGTGGCTGCTGACCAGTGGTACAACCAATGCAA
ATGCCTGGAAAAGCACCCTGGTTGGTCATGATACATTTACCAAAGTTAAA
CCGAGCGCAGCGAGCGGTGGTCATCATCATCACCATCAT
Amino Acid Sequence of Rituximab-scFv-V2122
(SEQ ID NO: 42)
MKYLLPTAAAGLLLLAAQPAMAQIVLSQSPAILSASPGEKYTMTCRASSS
VSYIHWFQQKPGSSPKPWIYATSNLASGVPVRFSGSGSGTSYSLTISRVE
AEDAATYYCQQWTSNPPTFGGGTKLEIKGGGGSGGGGSGGGGSGGGGSQV
QLQQPGAELVKPGASVKMSCKASGYTFTSYNMHWVKQTPGRGLEWIGAIY
PGNGDTSYNQKFKGKATLTADKSSSTAYMQLSSLTSEDSAVYYCARSTYY
GGDWYFNVWGAGTTVTVSAGGGGSGGGGAEAGITGTWSDQLGDTFIVTAG
ADGALTGTYENAVGNAESRYVLTGRYDSAPATDGSGTALGWTVAWKNNSK
NAHSATTWSGQYVGGADAKINTQWLLTSGTTNANAWKSTLVGHDTFTKVK
PSAASGGHHHHHH
(2) Expression and Partial Purification of Protein
Rituximab-scFv-V2122 protein was expressed in Escherichia coli. More specifically, pETDuet-1(skp)Rituximab-scFv-V2122, which is a plasmid vector, was introduced into BL21 (DE3) (Nippon Gene Co., Ltd.) for transformation. The transformed Escherichia coli was cultured overnight in 100 mL of 2×YT medium at 37° C. Next, 20 mL of the preculture liquid was added to 1 L of 2×YT medium, and the mixture was cultured at 37° C. Upon confirming OD600nm=2.0, IPTG and Triton X-100 were added while adjusting the final concentration to 1 mM and 1%, respectively, and the mixture was cultured for 18 hours to 24 hours at 20° C. The supernatant of culture was then collected by centrifugation, and 4 L of supernatant was pooled. Next, the protein was partially purified using Ni-NTA resin. More specifically, 5 mL equivalent of cOomplete His-Tag Purification Resin (Roche) was added to the 4-L pool, the mixture was kept stirred using a stirrer overnight at 4° C. so as to allow a binding process to proceed. The resin was then collected into a column, washed with 50 mL of washing buffer (50 mM Tris-HCl, 0.2 M NaCl, 1 mM EDTA, 5 mM imidazole, pH8.0), and then eluted with 40 mL of elution buffer (50 mM Tris-HCl, 0.2 M NaCl, 1 mM EDTA, 400 mM imidazole, pH8.0). The eluate was concentrated using Vivaspin Turbo 15, MWCO=30,000 (Sartorius AG) to 1 to 3 mL, and then stored frozen (−80° C.) (
(3) Purification of Rituximab-scFv-V2122 Protein Through Protein L Column
The protein was further purified by using Protein L 1 mL column (HiTrap L (GE Healthcare BioScience Corp.)). More specifically, the column was equilibrated using 10 column volumes of PBS, and a sample diluted 2-fold with PBS was applied. The column was washed with 10 column volumes of PBS, and then eluted with 10 column volumes of 10 mM glycine-HCl buffer pH2.5. The buffer in the eluate was immediately replaced with PBS using PD10 column, and then concentrated using Vivaspin Turbo 15, MWCO=100,000 (Sartorius AG) to 0.3 to 1 mL, and then stored cool (
(4) Fluorescent Labeling
The thus purified Rituximab-scFv-V2122 was preliminarily mixed with Psyche F-IRDye 800 (Compound 44 in Example) dissolved in DMSO (final concentration is ten-fold molar concentration), and incubated on ice for 10 minutes. The buffer was then replaced with Japanese Pharmacopoeia physiological saline (Otsuka Pharmaceutical Co., Ltd.) using Zeba Spin Desalting Column (Thermo Fisher Scientific Inc.).
(5) Flow Cytometer
Ramos cell (human Burkitt lymphoma-derived cell) (JCR Cell Bank), in which human CD20 antigen is abundantly expressed, was collected by centrifugation. The cells were suspended in PBS (1×106 cells/mL), and incubated with an antibody to be tested (0 nM, 0.5 nM, 5 nM, 50 nM, 100 nM) at room temperature for 30 minutes. The cells were washed twice with PBS, added with 0.1 mL of anti 6×His-tag antibody Alexa Flour 488 (500 ng/mL), and the mixture was incubated at room temperature for 30 minutes. The cells were washed twice with PBS, and binding mode and specificity of the test antibody were evaluated using guava easyCyte (Merck Millipore), according to the user's manual available from the manufacturer (
(6) Heterotransplantation Model
Ramos cell suspension and Matrigel Matrix (Corning) were mixed in a ratio of 1:1 (5×106 cells/0.1 mL), and 0.1 mL of the mixed liquid was administered subcutaneously in the left side of 5 to 6-week-old female nude mice (Sankyo Labo Service Corporation, Inc.). The mice were bred for several weeks to produce tumor. One week before imaging, the feed was switched to a low fluorescence feed (iVid #1, Oriental Yeast Co., Ltd.) and the breeding was continued. Mice in which an average tumor volume had reached 100 to 600 mm3 were used for fluorescent imaging test.
(7) In Vivo Imaging
Rituximab-scFv-V2122 antibody (25 μg, 50 μg, 100 μg), preliminarily labeled with fluorescence by reacting it with Psyche F-IRDye 800 (Compound 44 in Example), was intravenously administered to nude mice having established human Burkitt lymphoma Ramos. For investigation into accumulation in tumor, accumulation of IRDye 800 in the tumor was evaluated 2, 24 and 48 hours after the administration, using in vivo photo-imaging instrument Clairvivo OPT plus (Shimadzu Corporation) (
(8) Results
First; as shown in
(1) Expression and Partial Purification of Protein
Anti-epiregulin scFv-V2122 protein was expressed using anti-epiregulin scFv-V2122 expression vector described in Example 10 (1). More specifically, pETDuet-epiregulin-scFvV2122 skp, which is a plasmid vector, was introduced into BL21 (DE3) (Nippon Gene Co., Ltd.) for transformation. The transformed Escherichia coli was cultured overnight in 100 mL of 2×YT medium (Difco Laboratories) at 37° C. Next, 20 mL of the preculture liquid was added to 1 L of 2×YT medium, and the mixture was cultured at 37° C. Upon confirming OD600nm=2.0, IPTG and Triton X-100 were added adjusting the final concentration to 1 mM and 1%, respectively, and the mixture was cultured for 18 hours to 24 hours at 20° C. The supernatant of culture was then collected by centrifugation, and 4 L of supernatant was pooled.
Next, the protein was partially purified using Ni-NTA resin. More specifically, 5 mL of cOomplete His-Tag Purification Resin (Roche) was added to 4 L of the pooled sample, the mixture was kept stirred using a stirrer overnight at 4° C. so as to allow a binding process to proceed. The resin was then collected into a column, washed with 50 mL of washing buffer (50 mM Tris-HCl, 0.2 M NaCl, 1 mM EDTA, 5 mM imidazole, pH8.0), and then eluted with 40 mL of elution buffer (50 mM Tris-HCl, 0.2 M NaCl, 1 mM EDTA, 400 mM imidazole, pH8.0). The eluate was concentrated using Vivaspin Turbo 15, MWCO=30,000 (Sartorius AG) to 1 to 3 mL, and then stored frozen (−80° C.) (
(2) Purification Through Protein L Column
The protein was further purified by using Protein L 1 mL column (HiTrap L (GE Healthcare BioScience Corp.)). More specifically, the column was equilibrated using 10 column volumes of PBS, and a sample diluted 2-fold with PBS was applied. The column was washed with 10 column volumes of PBS, and then eluted with 10 column volumes of 10 mM glycine-HCl buffer pH2.5. The buffer in the eluate was immediately replaced with PBS using PD10 column, and then concentrated using Vivaspin Turbo 15, MWCO=100,000 (Sartorius AG) to 0.3 to 1 mL, and then stored cool (
(3) Fluorescent Labeling
The thus purified anti-epiregulin scFv-V2122 was mixed with Psyche F-IRDye 800 (Compound 44 in Example) dissolved in DMSO (final concentration was ten-fold molar concentration), and the mixture was incubated on ice for 10 minutes. The buffer was then replaced with Japanese Pharmacopoeia physiological saline (Otsuka Pharmaceutical Co., Ltd.) using Zeba Spin Desalting Column (Thermo Fisher Scientific Inc.) and was stored under cooling. Epiregulin IgG was labeled using ICG Labeling Kit-NH2 (Dojindo Laboratories).
(4) Heterotransplantation Model
Suspension liquid of human colorectal cancer-derived DLD1 cell and Matrigel Matrix (Corning) were mixed in a ratio of 1:1 (5×106 cells/0.1 mL), and 0.1 mL of the mixed liquid was administered subcutaneously in the left side of 5 to 6-week-old female nude mice (Sankyo Labo Service Corporation, Inc.). The mice were bred for several weeks to produce tumor. One week before imaging, the feed was switched to a low fluorescence feed (iVid #1, Oriental Yeast Co., Ltd.) and the breeding was continued. Mice in which an average tumor volume had reached 100 to 600 mm3 were used for fluorescent imaging test.
(5) In Vivo Imaging
Anti-epiregulin scFv-V2122 antibody (25 μg, 50 μg, 100 μg) preliminarily labeled with fluorescence by allowing it to react with Psyche F-IRDye 800 (Compound 44 in Example), or fluorescent-labeled epiregulin IgG (50 μg) was intravenously administered to nude mice having established DLD1 tumor. For investigation into accumulation in tumor, accumulation of IRDye 800 in the tumor was evaluated 2, 24 and 48 hours after the administration, using in vivo photo-imaging instrument Clairvivo OPT plus (Shimadzu Corporation) (
(6) Results
First, as shown in
Sugiyama, Akira, Shimizu, Yohei, Kanai, Motomu, Kodama, Tatsuhiko, Inoue, Tsuyoshi, Doi, Hirofumi, Mizohata, Eiichi, Kawato, Tatsuya, Meshizuka, Tomohiro, Takasu, Noriaki, Takatsu, Mari
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 6153442, | May 20 1998 | Siemens Healthcare Diagnostics Inc | Reagents and methods for specific binding assays |
| 7842475, | Jan 08 2008 | Siemens Healthcare Diagnostics Inc | Stabilization of solid support assay reagents |
| 9670255, | Feb 20 2013 | SAVID THERAPEUTICS INC | Modified biotin, mutant streptavidin, and use thereof |
| 20020068367, | |||
| 20090176213, | |||
| 20120039879, | |||
| 20140011255, | |||
| CN103298949, | |||
| CN104995196, | |||
| EP1304331, | |||
| EP2335721, | |||
| EP2960243, | |||
| JP2006275865, | |||
| JP6096371, | |||
| WO2009089262, | |||
| WO2010095455, | |||
| WO2012023579, | |||
| WO2012023580, | |||
| WO2012058635, | |||
| WO2014129446, |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Oct 13 2016 | SUGIYAMA, AKIRA | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 13 2016 | KODAMA, TATSUHIKO | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 14 2016 | KAWATO, TATSUYA | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 14 2016 | KANAI, MOTOMU | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 14 2016 | TAKASU, NORIAKI | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 14 2016 | MIZOHATA, EIICHI | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 14 2016 | DOI, HIROFUMI | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 14 2016 | SHIMIZU, YOHEI | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 15 2016 | INOUE, TSUYOSHI | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 17 2016 | MESHIZUKA, TOMOHIRO | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Oct 18 2016 | TAKATSU, MARI | SAVID THERAPEUTICS INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 049767 | /0288 | |
| Jul 16 2019 | SAVID THERAPEUTICS INC. | (assignment on the face of the patent) | / |
| Date | Maintenance Fee Events |
| Date | Maintenance Schedule |
| Sep 21 2024 | 4 years fee payment window open |
| Mar 21 2025 | 6 months grace period start (w surcharge) |
| Sep 21 2025 | patent expiry (for year 4) |
| Sep 21 2027 | 2 years to revive unintentionally abandoned end. (for year 4) |
| Sep 21 2028 | 8 years fee payment window open |
| Mar 21 2029 | 6 months grace period start (w surcharge) |
| Sep 21 2029 | patent expiry (for year 8) |
| Sep 21 2031 | 2 years to revive unintentionally abandoned end. (for year 8) |
| Sep 21 2032 | 12 years fee payment window open |
| Mar 21 2033 | 6 months grace period start (w surcharge) |
| Sep 21 2033 | patent expiry (for year 12) |
| Sep 21 2035 | 2 years to revive unintentionally abandoned end. (for year 12) |